PRECIPIO INC
NPI 1841375094
Clinical Medical Laboratory in New Haven, CT

Q: What is Precipio Inc's NPI number?

The NPI number for Precipio Inc is 1841375094. It was assigned to this organization in the NPPES registry on October 26, 2006.

Q: What is Precipio Inc's specialty?

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

Q: When was this NPI record last updated?

The NPPES record for Precipio Inc was last updated on March 28, 2023. NPI Profile syncs weekly with the NPPES registry data releases published by CMS. This NPI record was last updated 3 years 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.

Active since October 26, 2006

4 SCIENCE PARK STE 3, NEW HAVEN, CT 06511(203) 787-7888(203) 901-1289 Get Directions Write a Review

NPPES record last updated: March 28, 2023. Verified against the NPPES registry weekly; last sync: October 04, 2026.

Record update history: Mar 28, 2023, Oct 21, 2019, Oct 1, 2015 (3 updates tracked since 2015).

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About Precipio Inc NPPES

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

PRECIPIO INC (NPI 1841375094) is a healthcare organization registered as a clinical medical laboratory in New Haven, Connecticut and active in the NPI registry since October 2006. The organization lists Mehmed Iljazi, Billing Manager, as its authorized official.

NPPES Registry Identity

NPI1841375094

Entity TypeOrganization

Primary Taxonomy291U00000X

Legal Business NamePRECIPIO INC

Location Address4 SCIENCE PARK STE 3New Haven, CT 06511-1962

Mailing Address4 Science Park Ste 3New Haven, CT 06511-1962 · (203) 787-7888 · Fax (203) 901-1289

Phone(203) 787-7888

Fax(203) 901-1289

Organization SubpartNo

Authorized OfficialMehmed IljaziBilling Manager · (203) 787-7888

Enumeration DateOctober 26, 2006

Last NPPES UpdateMarch 28, 20233 updates tracked since enumeration

NPPES CertifiedMarch 28, 2023

✔ NPI 1841375094 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.

4 SCIENCE PARK STE 3, New Haven, CT 06511

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Other Identifiers 1

Other30057NE · Blue Cross Blue Shield

Accepted Insurance

The full list of accepted plans is on the Insurance tab. Issuers include Blue Cross and Blue Shield of Texas, Blue Cross Blue Shield of Michigan Mutual Insurance Company.Insurance ›

Areas of Expertise CMS Part B claims 42

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.

45,378 services1,659 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.

3,762 services923 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.

2,874 services327 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.

2,737 services371 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.

2,351 services2,121 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.

1,859 services1,663 patients

Molecular pathology procedure; physician interpretation and report G0452

A molecular pathology procedure involves analyzing your body's cells at a molecular level to identify any abnormalities. This can help detect diseases early. A physician will interpret the results and provide a detailed report, explaining the findings clearly.

1,491 services1,302 patients

Microscopic genetic analysis of tissue, manual, each additional procedure 88369

Microscopic genetic analysis of tissue is a procedure where a small sample of your body tissue is examined under a microscope. This is done to study the genes in your cells. If more than one procedure is needed, each additional one involves repeating this process. It's a key part of diagnosing and managing many health conditions.

1,175 services459 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.

682 services374 patients

Microscopic genetic analysis of tissue, manual, initial procedure 88368

Microscopic genetic analysis of tissue is a test that examines your cells under a microscope. This helps to identify any genetic changes that could be causing health issues. It's the first step in a series of tests to pinpoint the root cause of your symptoms.

669 services626 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.

632 services344 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.

549 services400 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.

536 services397 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.

535 services396 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.

441 services435 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.

420 services405 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.

409 services394 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.

407 services392 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.

402 services387 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.

400 services395 patients

Gene analysis (mpl proto-oncogene, thrombopoietin receptor) for detection of common variants 81338

Gene analysis for the MPL proto-oncogene, thrombopoietin receptor, is a test that looks for common genetic variants. This helps in understanding certain health conditions related to blood cell production. It's a non-invasive procedure, involving a simple blood draw.

400 services395 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.

399 services394 patients

Chromosome analysis for genetic defects, count 15-20 cells 88262

Chromosome analysis is a test that examines your body's cell structure to detect any genetic abnormalities. In this procedure, 15-20 cells are studied to identify any unusual changes that may indicate a genetic disorder. This helps in early detection and management of potential health issues.

397 services384 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.

350 services334 patients

Genetic sequencing localization, each multiplex procedure 88366

Genetic sequencing localization, each multiplex procedure, is a method used to identify specific areas in your DNA. It involves studying multiple genes at once to detect variations or mutations that might be linked to certain health conditions. This process helps in understanding your genetic makeup and potential health risks.

287 services141 patients

Gene analysis (splicing factor [3b] subunit b1) for detection of common variants 81347

Gene analysis for splicing factor 3b subunit b1 detects common variants. It's a test that examines your DNA, specifically the SF3B1 gene, to identify any changes or mutations. These variations can sometimes be linked to certain health conditions.

260 services251 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.

155 services147 patients

Molecular pathology procedure 81479

A molecular pathology procedure is a specialized lab test that analyzes your genes at a molecular level. It helps identify genetic variations or changes that may affect your health. This information can assist in diagnosing, monitoring, and deciding treatment for certain conditions.

142 services135 patients

Chromosome analysis for genetic defects, additional cells counted, each study 88285

Chromosome analysis is a study that examines your body's chromosomes to identify any genetic defects. In some cases, additional cells may be counted to ensure accuracy. This can provide valuable information about potential health risks and inform treatment decisions.

119 services118 patients

Gene analysis (additional sex combs like 1, transcriptional regulator) targeted sequence analysis 81176

Gene analysis, specifically for the additional sex combs like 1, transcriptional regulator, is a targeted sequence analysis. This test examines specific regions of a gene to identify any changes or mutations. These changes can help understand certain health conditions and guide future health decisions.

106 services105 patients

Gene analysis (runt related transcription factor 1) targeted sequence analysis 81334

Gene analysis for RUNX1 involves studying a specific part of your DNA. This test helps identify changes or mutations in the RUNX1 gene, which can provide insights into certain health conditions. It's like reading a book to find any spelling mistakes that could change the story.

106 services105 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.

89 services59 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.

84 services81 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.

64 services63 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.

37 services36 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.

37 services36 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.

36 services35 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.

36 services35 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.

36 services35 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.

36 services35 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.

36 services35 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.

19 services19 patients

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 Precipio Inc's NPI number?

The NPI number for Precipio Inc is 1841375094. It was assigned to this organization in the NPPES registry on October 26, 2006.

Where is Precipio Inc located?

Precipio Inc is located at 4 Science Park Ste 3, New Haven, CT 06511. The listed phone number is (203) 787-7888.

What is Precipio Inc's specialty?

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

What insurance does Precipio Inc accept?

Health plans from Blue Cross Blue Shield of Michigan Mutual Insurance Company and Blue Cross and Blue Shield of Texas list Precipio 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 Precipio Inc was last updated on March 28, 2023. NPI Profile syncs weekly with the NPPES registry data releases published by CMS. This NPI record was last updated 3 years 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.