NEOGENOMICS LABORATORIES INC
NPI 1396408829
Clinical Medical Laboratory in Fort Myers, FL

Q: What is Neogenomics Laboratories Inc's NPI number?

The NPI number for Neogenomics Laboratories Inc is 1396408829. It was assigned to this organization in the NPPES registry on October 21, 2021.

Q: What is Neogenomics Laboratories Inc's specialty?

The primary specialty registered for this NPI is Clinical Medical Laboratory with taxonomy code 291U00000X.

Active since October 21, 2021

9490 NEOGENOMICS WAY, FORT MYERS, FL 33912(866) 776-5904(888) 443-4153 Get Directions Write a Review

NPPES record last updated: March 3, 2026. Verified against the NPPES registry weekly; last sync: August 09, 2026.

Record update history: Mar 3, 2026, Dec 9, 2024, Jan 6, 2023 and 2 more (5 updates tracked since 2021).

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About Neogenomics Laboratories Inc NPPES

Official registry information on file with the National Plan and Provider Enumeration System.

NEOGENOMICS LABORATORIES INC (NPI 1396408829) is a healthcare organization registered as a clinical medical laboratory in Fort Myers, Florida and active in the NPI registry since October 2021. The organization lists Abhishek Jain, Chief Financial Officer, as its authorized official.

NPPES Registry Identity

NPI1396408829

Entity TypeOrganization

Primary Taxonomy291U00000X

Legal Business NameNEOGENOMICS LABORATORIES INC

Location Address9490 NEOGENOMICS WAYFort Myers, FL 33912

Mailing AddressPo Box 947365Atlanta, GA 30394-7365 · (866) 776-5907 · Fax (888) 443-4153

Phone(866) 776-5904

Fax(888) 443-4153

Organization SubpartNo

Authorized OfficialAbhishek JainChief Financial Officer · (866) 776-5907

Enumeration DateOctober 21, 2021

Last NPPES UpdateMarch 3, 20265 updates tracked since enumeration

NPPES CertifiedMarch 3, 2026

✔ NPI 1396408829 is a valid, active identifier and passes the ISO check-digit test.

Specialties & Licenses

★ Primary SpecialtyClinical Medical LaboratoryLaboratories

Taxonomy Code291U00000X

Definition

(1) A clinical laboratory is a facility for the biological, microbiological, serological, chemical, immunohematological, hematological, biophysical, cytological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of any disease or impairment of, human beings. These examinations also include procedures to determine, measure, or otherwise describe the presence or absence of various substances or organisms in the body. Facilities only collecting or preparing specimens (or both) or only serving as a mailing service and not performing testing are not considered clinical laboratories. (2) Any facility that examines materials from the human body for purposes of providing information for the diagnosis, prevention, or treatment of any disease or impairment of, or the assessment of, the health of human beings. Typical divisions of a clinical laboratory include hematology, cytology, bacteriology, histology, biochemistry, medical toxicology, and serology.

9490 NEOGENOMICS WAY, Fort Myers, FL 33912

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Accepted Insurance

The full list of accepted plans is on the Insurance tab. Issuers include Ambetter from Absolute Total Care, Ambetter from Arizona Complete Health, Ambetter from Arkansas Health & Wellness and more.Insurance ›

Areas of Expertise CMS Part B claims 79

Services this provider delivered to Medicare fee-for-service patients, from the CMS Medicare utilization data. Higher counts generally reflect more experience with a service; care delivered outside Medicare is not included.

Flow cytometry technique for dna or cell analysis, each additional marker 88185

Flow cytometry is a technique that helps analyze the physical and chemical characteristics of cells or particles. When an additional marker is used, it aids in identifying specific cell types or stages of disease. This helps in precise diagnosis and treatment planning.

71,835 services2,947 patients

Microscopic genetic analysis of tissue, computer-assisted technology, initial procedure, each multiplex procedure 88374

This procedure involves analyzing tissue at a genetic level using a microscope and advanced computer technology. The initial process involves the collection and preparation of tissue samples. Each multiplex procedure refers to the simultaneous testing of multiple genetic markers to identify abnormalities.

21,715 services5,971 patients

Microscopic genetic analysis of tissue, computer-assisted technology, initial procedure, each multiplex procedure 88374

12,896 services3,516 patients

Special stained specimen slides to examine tissue, each additional procedure 88341

Special stained specimen slides are used to analyze tissue in detail. In this process, extra procedures may be needed for a more thorough examination. These involve applying special stains to the tissue on slides, enhancing specific elements for closer study.

9,794 services1,834 patients

Special stained specimen slides to examine tissue, each additional procedure 88341

6,483 services896 patients

Flow cytometry technique for dna or cell analysis, 16 or more markers 88189

Flow cytometry is a method used to measure and analyze cells. It uses a beam of light to detect up to 16 or more markers on cells, helping to identify their type, function, or abnormalities. This technique aids in diagnosing various health conditions.

4,481 services4,258 patients

Translocation analysis (bcr/abl1) major breakpoint 81206

Translocation analysis (bcr/abl1) major breakpoint is a test that checks for a specific gene rearrangement in your cells. This rearrangement is often seen in certain types of leukemia. The test helps doctors diagnose and monitor treatment for these conditions.

4,051 services2,278 patients

Interpretation and report of genetic testing 88291

Interpretation and report of genetic testing involves analyzing your DNA to look for changes that could indicate a risk for certain health conditions. The results are then compiled into a report, which provides insights about your genetic health.

4,029 services3,955 patients

Special stained specimen slides to examine tissue including interpretation and report 88313

Special stained specimen slides are used to examine tissue samples. This involves applying special dyes to the tissue, which helps to highlight certain features under a microscope. The findings are then interpreted and a report is provided. This can aid in diagnosing various health conditions.

4,028 services1,053 patients

Special stained specimen slides to examine tissue, initial procedure 88342

This procedure involves the use of specially stained slides to examine tissue samples. The initial process involves obtaining a small tissue sample from your body. This sample is then placed on a slide and stained with special dyes to highlight different structures and elements. The stained slide is then examined under a microscope to help diagnose any potential health issues.

3,972 services2,889 patients

Microscopic genetic analysis of tumor, manual 88360

Microscopic genetic analysis of a tumor involves examining your tumor's genes under a microscope. This helps identify specific genetic changes in the tumor cells. This information can aid in diagnosing, predicting disease progression, and determining the most effective treatment options.

3,900 services3,282 patients

Microscopic genetic analysis of tumor, using computer-assisted technology 88361

Microscopic genetic analysis of a tumor uses advanced computer technology to examine the genetic makeup of the tumor cells. This helps to understand the tumor better and tailor a treatment plan. It's a non-invasive procedure and provides valuable insights for your healthcare team.

3,307 services1,168 patients

Flow cytometry technique for dna or cell analysis, first marker 88184

Flow cytometry is a technique used to examine microscopic particles, like cells or DNA. It employs a beam of light to detect and measure physical and chemical characteristics of these particles. The 'first marker' refers to a specific characteristic or feature used to identify a particular cell or particle.

3,221 services2,973 patients

Microscopic genetic analysis of tumor, manual 88360

3,091 services2,565 patients

Tissue culture for tumor disorders of bone marrow and blood cells 88237

Tissue culture for tumor disorders of bone marrow and blood cells is a lab process where your cells are grown in a controlled environment. The aim is to detect and study abnormal cells, such as cancer, in your bone marrow or blood. This helps in planning effective treatment.

2,888 services1,969 patients

Gene analysis (janus kinase 2) variant 81270

Gene analysis (Janus Kinase 2 variant) is a test that examines your DNA to identify any changes in the JAK2 gene. This gene is crucial for blood cell production. If it's mutated, it can lead to various blood disorders. The test helps in diagnosing these conditions.

2,711 services2,653 patients

Special stained specimen slides to examine tissue including interpretation and report 88313

2,644 services701 patients

Microscopic genetic analysis of tumor, using computer-assisted technology 88361

2,469 services887 patients

Special stained specimen slides to examine tissue, initial procedure 88342

2,151 services1,626 patients

Gene analysis (janus kinase 2) targeted sequence analysis 81279

Gene analysis, specifically Janus Kinase 2 (JAK2) targeted sequence analysis, is a lab test that studies a specific gene in your body. It helps identify changes or mutations in the JAK2 gene, which can be linked to certain health conditions. This analysis is performed on a blood or bone marrow sample.

1,974 services1,947 patients

Pathology examination of tissue using a microscope, intermediate complexity 88305

A pathology examination of tissue with intermediate complexity involves studying a small sample of your body tissue under a microscope. This helps in identifying any abnormal cells or signs of disease. It's a detailed process requiring expert analysis to ensure accurate results.

1,966 services986 patients

Genomic sequence analysis panel of dna or combined dna and rna of 5-50 genes associated with blood and lymphatic system disorders 81450

This test examines your DNA to identify any genetic changes that could indicate a risk for blood-related cancers. It's a simple process where a sample of your blood or saliva is taken and sent to a lab for detailed examination.

1,875 services1,839 patients

Microscopic genetic analysis of tissue, manual, each additional multiplex stain procedure 88377

Microscopic genetic analysis of tissue is a detailed lab process that examines your cells' genetic material. If more than one stain procedure is needed, it's termed an 'additional multiplex stain procedure'. This helps to highlight different components within your cells, aiding in accurate diagnosis and treatment planning.

1,844 services923 patients

Gene analysis (calreticulin), common variants 81219

Gene analysis of calreticulin, common variants, is a test that looks at specific genes to identify changes that may cause certain health issues. It helps in understanding your genetic makeup and potential health risks. It's a simple procedure involving a blood or saliva sample.

1,829 services1,807 patients

Translocation analysis (bcr/abl1) minor breakpoint 81207

Translocation analysis (bcr/abl1) minor breakpoint is a genetic test that identifies specific changes in chromosomes. It's used to diagnose certain types of blood cancers. The test detects rearrangements of genetic material, aiding in the treatment plan.

1,781 services1,441 patients

Gene analysis (mpl proto-oncogene, thrombopoietin receptor) sequence analysis of exon 10 81339

Gene analysis of the MPL proto-oncogene, thrombopoietin receptor, specifically sequence analysis of exon 10, is a procedure that studies a specific part of your DNA. It helps to identify any changes or mutations that may contribute to certain blood disorders.

1,761 services1,743 patients

Chromosome analysis for genetic defects, analyze 20-25 cells 88264

Chromosome analysis is a test that evaluates your cells to check for genetic defects. In this procedure, 20-25 cells are examined under a microscope to identify any abnormalities. This information can help in diagnosing certain genetic conditions and guide treatment plans.

1,480 services1,441 patients

Bone marrow, smear interpretation 85097

Bone marrow smear interpretation is a procedure where a small sample of your bone marrow is taken and examined under a microscope. This helps doctors identify any abnormal cells or signs of diseases such as anemia, leukemia, or infections. It's a crucial step in diagnosing various blood disorders.

1,465 services1,422 patients

Microscopic genetic analysis of tissue, manual, each additional multiplex stain procedure 88377

1,155 services578 patients

Pathology examination of tissue using a microscope, intermediate complexity 88305

1,091 services596 patients

Preparation of tissue for examination by removing any calcium present 88311

This procedure involves treating tissue samples to remove any calcium, which can interfere with the examination. The tissue is soaked in a special solution that safely dissolves the calcium, leaving the tissue intact for accurate analysis. This helps in making precise diagnoses.

1,018 services952 patients

Gene rearrangement analysis (immunoglobulin heavy chain locus), variable region somatic mutation analysis 81263

Gene rearrangement analysis is a test that studies alterations in your immune system's DNA. Specifically, it evaluates the variable region somatic mutation in the immunoglobulin heavy chain locus, which helps understand your body's immune response.

870 services859 patients

Genetic sequencing localization, initial procedure 88365

Genetic sequencing localization is a process to identify where specific genes are located in your DNA. During the initial procedure, a sample of your cells is collected, usually through a simple swab or blood test. This data is then analyzed to pinpoint the location of certain genes. This can help understand your genetic makeup and potential health risks.

832 services628 patients

Gene rearrangement analysis detection abnormal clonal population (t cell antigen receptor gamma) 81342

Gene rearrangement analysis is a test that identifies abnormal T cells, which may indicate certain health conditions. It examines the T cell antigen receptor gamma, a key part of the immune system. It's like a detective looking for unusual patterns in your body's defenders.

815 services774 patients

Genetic sequencing localization, each additional procedure 88364

Genetic sequencing localization is a process where specific regions of your DNA are identified and studied. If you're having additional procedures, it simply means that more areas of your DNA are being examined. This helps to understand your genetic makeup better and can assist in identifying potential health risks.

767 services571 patients

Gene analysis (myeloid differentiation primary response 88) for p.leu265pro variant 81305

Gene analysis for the p.Leu265Pro variant involves studying the MYD88 gene, which plays a crucial role in immune response. This test helps identify changes in this gene that could potentially cause health issues. It's a non-invasive procedure, done through a blood sample.

691 services671 patients

Gene analysis (t cell antigen receptor beta) amplification methodology 81340

Gene analysis of T cell antigen receptor beta, using amplification methodology, is a process where the specific genes in your T cells are examined. This helps determine your body's immune response to diseases. It's a non-invasive procedure that aids in understanding your health better.

657 services625 patients

Gene analysis (tumor protein 53) targeted sequence analysis 81352

Gene analysis of tumor protein 53 involves studying a specific gene to understand its role in tumor growth. It helps to identify mutations that may contribute to cancer development. This knowledge can aid in creating a more personalized treatment plan.

647 services643 patients

Preparation of tissue for examination by removing any calcium present 88311

592 services579 patients

Gene analysis (v-raf murine sarcoma viral oncogene homolog b1) 81210

Gene analysis of v-raf murine sarcoma viral oncogene homolog b1 (BRAF) is a test that examines your DNA to identify changes or mutations in the BRAF gene. This information can help in diagnosing and treating certain diseases, including some types of cancer.

548 services539 patients

Genetic sequencing localization, initial procedure 88365

416 services328 patients

Genetic sequencing localization, each additional procedure 88364

408 services315 patients

Chromosome analysis for genetic defects, additional karyotypes, each study 88280

Chromosome analysis is a test that examines the number and structure of a person's chromosomes. This is done to identify any genetic defects. Additional karyotypes, each study, are further tests that look at the arrangement of these chromosomes. This can help in detecting genetic disorders.

282 services279 patients

Gene analysis (epidermal growth factor receptor), common variants 81235

Gene analysis of the epidermal growth factor receptor (EGFR) identifies common variants in this particular gene. This test helps in understanding your body's response to certain medications. It aids in personalized treatment planning, ensuring the most effective care.

276 services274 patients

Test for detecting genes associated with colon cancer, promoter methylation analysis 81288

Promoter methylation analysis is a test that helps identify certain genes linked to colon cancer. This process examines how the DNA in your cells is modified, which can indicate if you're at risk for this type of cancer.

260 services260 patients

Flow cytometry technique for dna or cell analysis, 9 to 15 markers 88188

Flow cytometry is a technique used to measure physical and chemical characteristics of cells or particles. It can analyze multiple markers (9 to 15) on a cell, helping to identify its type and function. This process can also examine DNA within cells for any abnormalities.

242 services240 patients

Genomic sequence analysis panel of dna or combined dna and rna of 51 or more genes associated with blood and lymphatic system disorders 81455

A genetic test for cancer is a medical test that checks your DNA for changes or mutations that might put you at risk for cancer. It's a proactive step to understand your health better and possibly take preventive measures if needed.

238 services233 patients

Surgical pathology consultation and report on referred material requiring preparation of slides 88323

A surgical pathology consultation involves the examination of tissue removed during surgery. The tissue is processed and slides are prepared for detailed study under a microscope. The findings are then compiled into a report to help guide your treatment plan.

205 services199 patients

Gene rearrangement analysis (immunoglobulin heavy chain locus) to detect abnormal clonal population amplified methodology 81261

Gene rearrangement analysis is a test that checks for abnormal cells in your body. It focuses on a specific part of your DNA, the immunoglobulin heavy chain locus. The test amplifies this area to detect if abnormal, or 'clonal', cells are present.

134 services132 patients

Gene rearrangement analysis (immunoglobulin kappa light chain locus) to detect abnormal clonal population 81264

Gene rearrangement analysis is a lab test performed on your cells. It studies the immunoglobulin kappa light chain locus, which is part of your immune system. The aim is to find any abnormal clones, which could indicate a health issue.

134 services132 patients

Microsatellite instability analysis 81301

Microsatellite instability analysis is a test that checks for abnormalities in your DNA, which could indicate a higher risk for certain types of cancers. It is a useful tool for early detection and prevention.

133 services131 patients

Cell examination of urine, manual 88120

A cell examination of urine, manually done, is a lab test where your urine is studied under a microscope. This helps identify any abnormal cells or substances in your urine, like bacteria or crystals, that could indicate health issues. It's a simple, non-invasive procedure.

127 services125 patients

Translocation analysis (bcr/abl1) other breakpoint 81208

Translocation analysis (bcr/abl1) is a genetic test that detects abnormal chromosome changes in your body's cells. This specific test identifies a unique breakpoint in the bcr/abl1 genes, often associated with certain types of blood disorders.

116 services106 patients

Gene analysis (abl proto-oncogene 1, non-receptor tyrosine kinase) 81170

Gene analysis of the ABL1 gene helps identify changes that may cause certain health issues. It involves examining the ABL1 gene, which makes a protein involved in cell division and communication. This test aids in diagnosing and managing treatment for these conditions.

115 services92 patients

Surgical pathology consultation and report on referred slides prepared elsewhere 88321

A surgical pathology consultation involves reviewing slides prepared at a different lab to confirm or clarify a diagnosis. It's a second opinion to ensure accuracy. A report with findings and interpretations is then provided for your doctor's reference.

106 services106 patients

Gene analysis (v-kit hardy-zuckerman 4 feline sarcoma viral oncogene homolog), targeted sequence 81272

Gene analysis of v-kit hardy-zuckerman 4 feline sarcoma viral oncogene homolog (KIT) is a test that studies a specific gene associated with cell growth and development. It helps in identifying any alterations in this gene that may lead to health issues.

98 services96 patients

Flow cytometry technique for dna or cell analysis, 2 to 8 markers 88187

Flow cytometry is a technique that helps analyze your cells and DNA. It uses lasers to identify and sort cells based on their properties, marked by up to 8 different markers. This helps in diagnosing and monitoring various health conditions.

84 services84 patients

Gene analysis (v-ki-ras2 kirsten rat sarcoma viral oncogene) variants in codons 12 and 13 81275

Gene analysis for v-ki-ras2 kirsten rat sarcoma viral oncogene variants in codons 12 and 13 is a test to identify specific changes in your genes. These changes could potentially indicate a higher risk for certain types of cancer.

78 services78 patients

Gene analysis (kirsten rat sarcoma viral oncogene homolog), additional variants 81276

Gene analysis of the Kirsten rat sarcoma viral oncogene homolog (KRAS) checks for extra variations in the KRAS gene. These variations may impact how your body responds to certain treatments. It's a non-invasive test, usually done on a blood or tissue sample.

78 services78 patients

Blood smear interpretation by physician with written report 85060

Blood smear interpretation is a lab test where your doctor examines a sample of your blood under a microscope. They look for abnormalities in your blood cells which can help diagnose various conditions. You'll receive a written report of the findings.

75 services75 patients

Gene analysis (nucleophosmin) exon 12 variants 81310

Gene analysis of nucleophosmin (exon 12 variants) is a specialized test used to identify alterations in a specific part of the NPM1 gene. These changes can help diagnose certain health conditions, particularly blood disorders. This test involves analyzing your DNA from a blood sample.

67 services39 patients

Translocation analysis (pml-rara regulated adaptor molecule 1) common breakpoint 81315

Translocation analysis (PML-RARA) is a genetic test that detects a specific change in your chromosomes, often associated with certain types of leukemia. The 'common breakpoint' refers to the exact spot where this change usually occurs. This test helps doctors diagnose and manage your condition.

64 services47 patients

Special stained specimen slides to identify organisms including interpretation and report 88312

This service involves coloring specimen slides in a special way to help identify organisms. The colors make different parts of the organism stand out. Afterward, a detailed interpretation and report on the findings are provided.

63 services37 patients

Special stained specimen slides to examine tissue, each multiplex procedure 88344

Special stained specimen slides are used to study tissue in detail. This multiplex procedure involves applying different dyes to the tissue sample on a slide to highlight specific elements. These colors help identify any abnormalities in the tissue, aiding in accurate diagnosis and treatment planning.

61 services27 patients

Gene analysis (neurotrophic receptor tyrosine kinase 1, 2, and 3) translocation analysis 81194

Gene analysis for neurotrophic receptor tyrosine kinase (NTRK) 1, 2, and 3 translocation is a test that checks for changes in your genes. These changes can impact how cells grow and divide, which can affect your health. It's a way to catch problems early.

59 services58 patients

Gene analysis (fms-related tyrosine kinase 3) internal tandem duplication variants 81245

Gene analysis for FLT3 internal tandem duplication variants is a process that examines your DNA to identify specific genetic changes. These changes might influence the development of certain conditions, like leukemia. The analysis aids in determining the most effective treatment plan.

51 services41 patients

Test for detecting genes associated with blood cancer 81246

This test identifies specific genes linked to blood cancer. It involves taking a blood sample, which is then analyzed in a lab. Changes in your genes can indicate a higher risk of developing blood cancer. Understanding these risks can aid in early detection and treatment planning.

51 services41 patients

Gene analysis (isocitrate dehydrogenase 1 [nadp+], soluble) for common variants 81120

Gene analysis for common variants of Isocitrate Dehydrogenase 1 (IDH1) is a procedure to identify changes in this specific gene. These changes can help predict certain health conditions and aid in personalized treatment planning.

47 services42 patients

Gene analysis (isocitrate dehydrogenase 2 [nadp+], mitochondrial) for common variants 81121

Gene analysis for isocitrate dehydrogenase 2 (IDH2), a mitochondrial enzyme, helps detect common genetic variants. This procedure aids in understanding your genetic makeup, which can influence health and disease risk. It's performed using a simple blood sample.

47 services42 patients

Gene analysis for cancer (neuroblastoma) 81311

Gene analysis for neuroblastoma is a test that studies your genes to identify abnormalities linked to this type of cancer. It helps doctors tailor treatment plans, potentially improving outcomes and reducing side effects.

40 services40 patients

Microscopic genetic analysis of tissue, computer-assisted technology, initial procedure 88367

This procedure involves the detailed study of your tissue's genetic makeup using a microscope and computer-assisted technology. It's the first step in a series of tests to understand your body better and provide appropriate care.

40 services38 patients

Microscopic genetic analysis of tissue, computer-assisted technology, initial procedure 88367

30 services28 patients

Gene analysis ((platelet-derived growth factor receptor, alpha polypeptide) targeted sequence 81314

Gene analysis for the platelet-derived growth factor receptor, alpha polypeptide (PDGFRA) involves sequencing this specific gene. The test can identify genetic changes or mutations that may cause certain health conditions. It's a non-invasive procedure that helps in early detection and personalized treatment plans.

28 services28 patients

Genomic sequence analysis panel of dna or combined dna and rna of 5-50 genes associated with solid organ abnormal growth of tissue 81445

This test identifies specific genes linked with body organ cancer. It's a simple process where a sample of your blood or saliva is collected. The sample is then analyzed in a lab to find any genetic changes that might increase cancer risk. It's a proactive step to manage your health.

26 services26 patients

Special stained specimen slides to identify organisms including interpretation and report 88312

26 services13 patients

Cell examination of urine, manual 88120

25 services25 patients

Gene analysis (o-6-methylguanine-dna methyltransferase) for promoter methylation 81287

Gene analysis of O-6-methylguanine-DNA methyltransferase (MGMT) for promoter methylation is a test that studies a specific gene in your DNA. This gene helps repair damaged DNA. The test checks for changes in the gene that may affect its function, which could influence disease treatment strategies.

18 services18 patients

Gene analysis (ccaat/enhancer binding protein [c/ebp], alpha) full gene sequence 81218

Gene analysis of the CCAAT/Enhancer Binding Protein (C/EBP), Alpha, involves studying the entire sequence of this particular gene. This can help identify variations or changes in the gene that might affect your health. This process is done in a lab using a sample of your cells.

15 services13 patients

Gene analysis (v-kit hardy-zuckerman 4 feline sarcoma viral oncogene homolog), d816 variants 81273

Gene analysis of the V-KIT Hardy-Zuckerman 4 Feline Sarcoma Viral Oncogene Homolog, D816 variants, is a test performed on your DNA. This test helps identify changes or mutations in the KIT gene, which can be associated with certain health conditions.

15 services15 patients

Other Providers at the Same Location NPPES

Providers registered at the same practice address, or within the immediate area, according to the NPPES registry.

DR. ANAHIT NOWROUZI M.D.

Pathology (Anatomic Pathology & Clinical Pathology)

9490 NEOGENOMICS WAY
FORT MYERS, FL 33912

Lee County (239) 768-0600

Frequently Asked Questions NPPES & CMS

Common questions about this NPI record, answered from the official NPPES registry and CMS datasets shown on this page.

What is Neogenomics Laboratories Inc's NPI number?

The NPI number for Neogenomics Laboratories Inc is 1396408829. It was assigned to this organization in the NPPES registry on October 21, 2021.

Where is Neogenomics Laboratories Inc located?

Neogenomics Laboratories Inc is located at 9490 Neogenomics Way, Fort Myers, FL 33912. The listed phone number is (866) 776-5904.

What is Neogenomics Laboratories Inc's specialty?

The primary specialty registered for this NPI is Clinical Medical Laboratory with taxonomy code 291U00000X.

What insurance does Neogenomics Laboratories Inc accept?

Health plans from Ambetter Health, Ambetter from Absolute Total Care, Ambetter from Arizona Complete Health, Ambetter from Arkansas Health & Wellness and Ambetter from Louisiana Healthcare Connections and 24 other insurers list Neogenomics Laboratories Inc as in-network in at least one marketplace plan. Coverage varies by plan and year; verify with the insurer or the provider before a visit.

When was this NPI record last updated?

The NPPES record for Neogenomics Laboratories Inc was last updated on March 3, 2026. NPI Profile syncs weekly with the NPPES registry data releases published by CMS. This NPI record was last updated 5 months ago. If this record has changed at CMS more recently, you can request an on-demand re-check against the live CMS registry, directly from this page.