OCEAN DIAGNOSTICS LLC
NPI 1366968224
Clinical Medical Laboratory in Miami, FL

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

The NPI number for Ocean Diagnostics LLC is 1366968224. It was assigned to this organization in the NPPES registry on August 22, 2017.

Q: What is Ocean Diagnostics LLC's specialty?

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

Active since August 22, 2017

1000 PARK CENTRE BLVD STE 136, MIAMI, FL 33169(888) 549-3499(754) 663-5043 Get Directions Write a Review

NPPES record last updated: March 6, 2024. Verified against the NPPES registry weekly; last sync: August 09, 2026.

Record update history: Mar 6, 2024, Jul 26, 2023, Jul 14, 2023 and 1 more (4 updates tracked since 2017).

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About Ocean Diagnostics Llc NPPES

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

OCEAN DIAGNOSTICS LLC (NPI 1366968224) is a healthcare organization registered as a clinical medical laboratory in Miami, Florida and active in the NPI registry since August 2017. The organization lists Leonid Zayonts, Owner, as its authorized official.

NPPES Registry Identity

NPI1366968224

Entity TypeOrganization

Primary Taxonomy291U00000X

Legal Business NameOCEAN DIAGNOSTICS LLC

Location Address1000 PARK CENTRE BLVD STE 136Miami, FL 33169-5373

Mailing Address1000 Park Centre Blvd Ste 136Miami, FL 33169-5373 · (888) 549-3499 · Fax (754) 663-5043

Phone(888) 549-3499

Fax(754) 663-5043

Organization SubpartNo

Authorized OfficialLeonid ZayontsOwner · (888) 549-3499

Enumeration DateAugust 22, 2017

Last NPPES UpdateMarch 6, 20244 updates tracked since enumeration

NPPES CertifiedMarch 6, 2024

✔ NPI 1366968224 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.

1000 PARK CENTRE BLVD STE 136, Miami, FL 33169

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Areas of Expertise CMS Part B claims 54

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.

2,942 services2,922 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.

2,594 services2,518 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.

2,590 services2,514 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.

2,586 services2,512 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.

2,263 services2,251 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.

2,058 services2,049 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.

2,051 services2,040 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.

1,984 services1,973 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.

1,816 services1,807 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.

1,816 services1,807 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.

1,812 services1,803 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.

1,811 services1,802 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.

1,810 services1,801 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.

1,807 services1,798 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.

1,807 services1,798 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.

1,803 services1,794 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.

1,755 services1,747 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.

1,619 services1,612 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.

1,614 services1,607 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.

1,575 services1,569 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.

814 services813 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.

814 services813 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.

798 services797 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.

792 services791 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.

792 services791 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.

791 services791 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.

790 services789 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.

790 services789 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.

790 services789 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.

788 services788 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.

788 services788 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.

788 services787 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.

787 services786 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.

786 services786 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.

782 services781 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.

781 services780 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.

779 services779 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.

779 services779 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.

778 services777 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.

775 services774 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.

762 services761 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.

744 services744 patients

Gene analysis (partner and localizer of brca2) targeted sequence analysis 81309

Gene analysis, specifically the partner and localizer of BRCA2 targeted sequence analysis, is a scientific procedure that studies specific parts of your DNA. It helps to identify if you have certain genetic changes that may increase your risk of developing specific health conditions.

634 services634 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.

613 services612 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.

132 services131 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.

129 services128 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.

114 services113 patients

Gene analysis (postmeiotic segregation increased 2 [s cerevisiae]) full sequence analysis 81317

Gene analysis, specifically postmeiotic segregation increased 2 (s cerevisiae) full sequence analysis, is a scientific procedure. It involves studying your entire genetic code to identify any changes or differences that could be related to certain health conditions. This is done in a lab, using a sample provided by you.

113 services112 patients

Gene analysis (prothrombin, coagulation factor ii) a variant 81240

Gene analysis for prothrombin (also known as coagulation factor II) is a test that examines your DNA to identify any variations in the prothrombin gene. These variations could potentially affect blood clotting, leading to an increased risk of certain health conditions.

24 services24 patients

Gene analysis (5, 10-methylenetetrahydrofolate reductase) common variants 81291

Gene analysis for 5,10-methylenetetrahydrofolate reductase (MTHFR) common variants is a test that looks at your DNA to identify any changes in the MTHFR gene. These changes can affect how your body processes certain vitamins, which could impact your overall health.

24 services24 patients

Gene analysis (cytochrome p450, family 2, subfamily c, polypeptide 19) common variants 81225

Gene analysis of cytochrome P450 2C19 common variants is a test that helps understand how your body processes certain medications. This can help your doctor tailor treatments specifically for you, improving their effectiveness and safety.

17 services17 patients

Gene analysis (dystrophin) 81161

Gene analysis for dystrophin is a test that examines the dystrophin gene, which plays a crucial role in muscle function. Errors in this gene can cause muscle disorders. This analysis helps detect any abnormalities, aiding in diagnosis and treatment planning.

12 services12 patients

Gene analysis (dihydropyrimidine dehydrogenase) for common variant 81232

Gene analysis for dihydropyrimidine dehydrogenase (DPD) common variant involves studying a specific gene in your body. This gene affects how your body processes certain medications. The test identifies any changes in this gene which may influence your response to these medications.

11 services11 patients

Gene analysis (solute carrier organic anion transporter family, member 1b1) for common variant 81328

Gene analysis for the solute carrier organic anion transporter family, member 1b1 (SLCO1B1), common variant, is a test that examines your DNA to identify variations in the SLCO1B1 gene. This gene plays a crucial role in the body's ability to process certain medications.

11 services11 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.

LIBERTY COMPOUNDING LLC

Pharmacy (Compounding Pharmacy)

1000 PARK CENTRE BLVD STE 136
MIAMI, FL 33169

Miami-Dade County (305) 749-6790

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 Ocean Diagnostics LLC's NPI number?

The NPI number for Ocean Diagnostics LLC is 1366968224. It was assigned to this organization in the NPPES registry on August 22, 2017.

Where is Ocean Diagnostics LLC located?

Ocean Diagnostics LLC is located at 1000 Park Centre Blvd Ste 136, Miami, FL 33169. The listed phone number is (888) 549-3499.

What is Ocean 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 Ocean Diagnostics LLC was last updated on March 6, 2024. NPI Profile syncs weekly with the NPPES registry data releases published by CMS. This NPI record was last updated 2 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.