EVEREST DIAGNOSTICS LLC
NPI 1609697085
Clinical Medical Laboratory in Pompano Beach, FL

Q: What is Everest Diagnostics LLC's NPI number?

The NPI number for Everest Diagnostics LLC is 1609697085. It was assigned to this organization in the NPPES registry on October 18, 2024.

Q: What is Everest Diagnostics LLC's specialty?

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

Active since October 18, 2024

2769 E ATLANTIC BLVD, POMPANO BEACH, FL 33062(754) 222-0333 Get Directions Write a Review

NPPES record last updated: March 13, 2025. Verified against the NPPES registry weekly; last sync: August 09, 2026.

On this page

About Everest Diagnostics Llc NPPES

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

EVEREST DIAGNOSTICS LLC (NPI 1609697085) is a healthcare organization registered as a clinical medical laboratory in Pompano Beach, Florida and active in the NPI registry since October 2024. The organization lists Maxim Pundik, Owner, as its authorized official.

NPPES Registry Identity

NPI1609697085

Entity TypeOrganization

Primary Taxonomy291U00000X

Legal Business NameEVEREST DIAGNOSTICS LLC

Location Address2769 E ATLANTIC BLVDPompano Beach, FL 33062-4941

Mailing Address2769 E Atlantic BlvdPompano Beach, FL 33062-4941

Phone(754) 222-0333

Organization SubpartNo

Authorized OfficialMaxim PundikOwner · (754) 222-0333

Enumeration DateOctober 18, 2024

Last NPPES UpdateMarch 13, 2025

NPPES CertifiedMarch 13, 2025

✔ NPI 1609697085 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.

2769 E ATLANTIC BLVD, Pompano Beach, FL 33062

Open in Google Maps ↗

Areas of Expertise CMS Part B claims 45

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.

Gene analysis (phosphatase and tensin homolog), full sequence analysis 81321

Gene analysis, specifically phosphatase and tensin homolog (PTEN) full sequence analysis, is a test that looks at your DNA to identify any changes in the PTEN gene. This gene helps control cell growth and division. Changes may lead to certain health conditions.

952 services950 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.

788 services779 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.

787 services778 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.

786 services778 patients

Gene analysis (tumor protein 53) full sequence analysis 81351

Gene analysis, specifically tumor protein 53 (TP53) full sequence analysis, is a test that examines the entire TP53 gene. This gene plays a key role in preventing cancer. If there are changes or mutations in this gene, it could lead to an increased risk of developing various types of cancer.

786 services778 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.

680 services680 patients

Gene analysis (phospholipase c gamma 2) for common variants 81320

Gene analysis for phospholipase C gamma 2 common variants is a test that checks for changes in the PLCG2 gene. These changes can sometimes lead to certain health conditions. The test uses a sample of your body's cells to analyze your DNA.

680 services680 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.

679 services679 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.

679 services679 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.

679 services679 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.

678 services678 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.

676 services676 patients

Gene analysis (telomerase reverse transcriptase) targeted sequence analysis 81345

Gene analysis of telomerase reverse transcriptase (TERT) involves studying a specific segment of your DNA. It helps understand how your body's cells age and multiply, which can be crucial in diagnosing and managing certain health conditions.

636 services636 patients

Gene analysis (coagulation factor v) leiden variant 81241

Gene analysis for the coagulation factor V Leiden variant is a test to identify a specific genetic mutation. This mutation can increase the risk of developing abnormal blood clots in veins. The test involves analyzing a sample of your DNA, usually taken from a blood sample.

615 services615 patients

Gene analysis (fanconi anemia, complementation group c) common variant 81242

Gene analysis for Fanconi Anemia, Complementation Group C, is a test that looks at your DNA to see if you have changes in a specific gene linked to this type of anemia. This can help determine if you have the condition or if you might pass it on to your children.

544 services544 patients

Gene analysis (bloom syndrome, recq helicase-like) 81209

Gene analysis for Bloom Syndrome involves studying the RECQ helicase-like gene. This gene is responsible for DNA repair. When it's not working properly, it can lead to Bloom Syndrome, a condition that increases the risk of developing various types of cancer.

537 services537 patients

Gene analysis (glucose-6-phosphate dehydrogenase) full sequence analysis 81249

Gene analysis for glucose-6-phosphate dehydrogenase (G6PD) involves studying your DNA to check for changes in the G6PD gene. This gene controls an enzyme that helps red blood cells function properly. Anomalies can cause health issues like anemia.

506 services506 patients

Gene analysis (cystic fibrosis transmembrane conductance regular) full gene sequence 81223

Gene analysis for cystic fibrosis involves examining the entire CFTR gene to identify any changes or mutations that could cause the disease. This can help in diagnosing and managing the condition effectively.

503 services503 patients

Gene analysis (partner and localizer of brca2) full sequence analysis 81307

Gene analysis, specifically for the partner and localizer of BRCA2, involves examining your genetic code to identify any changes in this particular gene. This gene is significant in maintaining the health of your cells. The full sequence analysis means we look at every part of this gene to ensure it's working properly.

503 services503 patients

Gene analysis (coagulation factor ix) full sequence analysis 81238

Gene analysis for coagulation factor IX is a process that examines your genes, specifically the one responsible for factor IX - a protein that helps blood clot. It can detect any changes or mutations in this gene, which could affect your body's ability to control bleeding.

498 services498 patients

Gene analysis (neurotrophic receptor tyrosine kinase 1) translocation analysis 81191

Gene analysis, specifically neurotrophic receptor tyrosine kinase 1 (NTRK1) translocation analysis, is a test that examines your genes for specific changes. These changes could potentially lead to certain health conditions. This analysis helps in providing personalized treatment plans.

419 services419 patients

Gene analysis (cch-type zinc finger nucleic acid binding protein) for abnormal alleles 81187

Gene analysis for CCH-type zinc finger nucleic acid binding protein checks for abnormal alleles. This process involves studying your DNA to identify any unusual genetic variations. These variations could potentially lead to health issues. It's a proactive step in understanding your body's genetic makeup.

418 services418 patients

Gene analysis (methyl cpg binding protein 2) full sequence analysis 81302

Gene analysis, specifically Methyl CpG Binding Protein 2 (MECP2) full sequence analysis, is a detailed examination of your DNA. This test focuses on the MECP2 gene, which plays a crucial role in nerve cell function and development. The results can help identify alterations or mutations that may cause certain health conditions.

402 services402 patients

Gene analysis (calcium voltage-gated channel subunit alpha1 a) of full sequence 81185

Gene analysis of the calcium voltage-gated channel subunit alpha1 a involves examining your DNA to understand how your body regulates calcium. This helps identify potential health risks related to calcium imbalances. It's a non-invasive procedure involving a simple blood or saliva sample.

401 services401 patients

Gene analysis (survival of motor neuron 1, telomeric) of full sequence 81336

Gene analysis of the full sequence of Survival of Motor Neuron 1 (telomeric) is a test that examines your DNA to identify any changes in this specific gene. These changes could indicate conditions like Spinal Muscular Atrophy. It's a non-invasive procedure.

391 services391 patients

Gene analysis (atropin 1) for abnormal alleles 81177

Gene analysis for Atropin 1 involves studying your DNA to identify any unusual genetic variations. This test helps in understanding your genetic makeup better, which can aid in diagnosing or predicting certain health conditions.

383 services383 patients

Gene analysis (fragile x syndrome, x-linked intellectual disability) for detection of abnormal alleles 81243

Gene analysis for Fragile X Mental Retardation involves studying your DNA to identify any abnormal changes or 'alleles'. This helps in detecting the presence of Fragile X syndrome, a genetic condition that can cause learning and behavioral challenges.

380 services380 patients

Gene analysis (peripheral myelin protein 22), full sequence analysis 81325

Gene analysis of peripheral myelin protein 22 involves studying the full sequence of this specific gene. This analysis helps identify any genetic variations that may lead to certain health conditions. It's a non-invasive test involving a simple blood draw or saliva sample.

379 services379 patients

Gene analysis (ataxin 1) for abnormal alleles 81178

Gene analysis of ataxin 1 involves studying your DNA to identify any abnormal versions of the ataxin 1 gene. This gene is associated with certain neurological disorders. The test helps in early detection and management of these conditions.

378 services378 patients

Gene analysis (ataxin 3) for abnormal alleles 81180

Gene analysis for ataxin 3 helps identify abnormal alleles, or variations, in the ataxin 3 gene. This gene plays a role in neurological function. If abnormal, it may indicate conditions like Machado-Joseph disease. The process involves analyzing a blood sample.

378 services378 patients

Gene analysis (ataxin 7) for abnormal alleles 81181

Gene analysis for ataxin 7 involves studying your DNA to identify any unusual changes in the ataxin 7 gene. These changes, known as abnormal alleles, can cause health conditions like spinocerebellar ataxia. The test helps in early detection and management.

378 services378 patients

Gene analysis (ataxin 10) for abnormal alleles 81183

Gene analysis for ataxin 10 involves examining your DNA to identify any abnormal versions of the ataxin 10 gene. These abnormalities could potentially cause certain health conditions. This test is non-invasive and helps in early detection and management of these conditions.

378 services378 patients

Gene analysis (hexosaminidase a) common variants 81255

Gene analysis of Hexosaminidase A common variants is a test that examines your DNA for changes in the Hex A gene. This gene is responsible for making an enzyme that breaks down certain substances in the body. Changes in this gene can lead to health issues.

378 services378 patients

Gene analysis (protein phosphatase 2 regulatory subunit bbeta) for abnormal alleles 81343

Gene analysis for the protein phosphatase 2 regulatory subunit Bbeta checks for unusual variations in your genes. This helps to identify potential health issues related to these genes. It's a simple, non-invasive test using a blood or saliva sample.

378 services378 patients

Gene analysis (cystatin b) of full sequence 81189

Gene analysis of the full sequence of Cystatin B is a test that examines your DNA to identify any changes in the Cystatin B gene. This gene is linked to certain health conditions. The analysis helps in diagnosing and tailoring treatment plans.

377 services377 patients

Gene analysis (ataxin 2) for abnormal alleles 81179

Gene analysis for ataxin 2 checks for alterations in the ATXN2 gene. This gene is responsible for producing a protein essential for normal cell functions. If abnormal, it may lead to certain neurological disorders. The test involves analyzing your DNA, typically obtained via a blood sample.

376 services376 patients

Gene analysis (frataxin) of full sequence 81286

Gene analysis of frataxin involves studying the entire sequence of the frataxin gene. This test helps identify any changes or mutations in the gene that may cause health issues, such as Friedreich's ataxia. It's a non-invasive procedure using a blood sample.

376 services376 patients

Gene analysis (tata box binding protein) for abnormal alleles 81344

Gene analysis for the TATA box binding protein checks for abnormal alleles or variations in your DNA. This analysis helps identify potential genetic conditions. It's done by examining a sample of your cells, typically obtained through a blood draw or a cheek swab.

376 services376 patients

Gene analysis (poly[a] binding protein nuclear 1) for abnormal alleles 81312

Gene analysis for Poly(A) Binding Protein Nuclear 1 (PABPN1) checks for abnormal alleles or variations in your DNA. This test can help identify genetic disorders caused by these variations. It's a non-invasive procedure, involving a simple blood or saliva sample.

375 services375 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.

107 services107 patients

Gene analysis (adenomatous polyposis coli), full gene sequence 81201

Gene analysis of the adenomatous polyposis coli (APC) involves studying the entire sequence of the APC gene. This test helps identify mutations that could lead to conditions like familial adenomatous polyposis. The procedure is non-invasive and uses a blood sample.

101 services101 patients

Gene analysis (breast cancer 1 and 2) of full sequence and analysis for duplication or deletion variants 81162

Gene analysis for breast cancer 1 and 2 involves studying your DNA to detect alterations that may increase your risk of developing certain health issues. This test analyzes the full sequence and checks for duplication or deletion variants.

88 services88 patients

Gene analysis (mutl homolog 1, colon cancer, nonpolyposis type 2) full sequence analysis 81292

Gene analysis, specifically for MUTL Homolog 1, linked to colon cancer, involves studying your DNA sequence. This helps identify any changes or mutations that might increase your risk of developing colon cancer. It's a preventive measure to manage potential health risks.

15 services15 patients

Gene analysis (muts homolog 2, colon cancer, nonpolyposis type 1) full sequence analysis 81295

Gene analysis (MUTYH) full sequence analysis is a test that examines your DNA to identify any changes linked to nonpolyposis colon cancer type 1. This can help determine your risk of developing this type of cancer.

14 services14 patients

Gene analysis (muts homolog 6 [e coli]) full sequence analysis 81298

Gene analysis, specifically MUTS Homolog 6 (E. coli) full sequence analysis, is a test that examines your DNA to identify changes in the MUTS Homolog 6 gene. This information helps doctors understand and manage potential health concerns.

11 services11 patients

Other Providers at the Same Location NPPES 2

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

BIOGROUP LABORATORY CORP

Clinical Medical Laboratory

2769 E ATLANTIC BLVD
POMPANO BEACH, FL 33062

Broward County (833) 265-2550

ELITE LABS LLC

Clinical Medical Laboratory

2769 E ATLANTIC BLVD
POMPANO BEACH, FL 33062

Broward County (954) 369-1306

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 Everest Diagnostics LLC's NPI number?

The NPI number for Everest Diagnostics LLC is 1609697085. It was assigned to this organization in the NPPES registry on October 18, 2024.

Where is Everest Diagnostics LLC located?

Everest Diagnostics LLC is located at 2769 E Atlantic Blvd, Pompano Beach, FL 33062. The listed phone number is (754) 222-0333.

What is Everest Diagnostics LLC's specialty?

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

When was this NPI record last updated?

The NPPES record for Everest Diagnostics LLC was last updated on March 13, 2025. NPI Profile syncs weekly with the NPPES registry data releases published by CMS. This NPI record was last updated 17 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.