PRECHECK HEALTH SERVICES INC
NPI 1760076061
Clinical Medical Laboratory in Miami, FL

Q: What is Precheck Health Services Inc's NPI number?

The NPI number for Precheck Health Services Inc is 1760076061. It was assigned to this organization in the NPPES registry on February 26, 2021.

Q: What is Precheck Health Services Inc's specialty?

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

Active since February 26, 2021CLIA 10D2210020 · Accreditation

100 BISCAYNE BLVD STE 1212, MIAMI, FL 33132(305) 203-4711 Get Directions Write a Review

NPPES record last updated: May 18, 2021. Verified against the NPPES registry weekly; last sync: July 19, 2026.

Record update history: May 18, 2021, Feb 26, 2021 (2 updates tracked since 2021).

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About Precheck Health Services Inc NPPES

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

PRECHECK HEALTH SERVICES INC (NPI 1760076061) is a healthcare organization registered as a clinical medical laboratory in Miami, Florida and active in the NPI registry since February 2021. The organization holds an CLIA Accreditation certificate valid through May 10, 2028 and lists Frank Gillen, Authorized Official, as its authorized official.

NPPES Registry Identity

NPI1760076061

Entity TypeOrganization

Primary Taxonomy291U00000X

Legal Business NamePRECHECK HEALTH SERVICES INC

Location Address100 BISCAYNE BLVD STE 1212Miami, FL 33132-2309

Mailing Address100 Biscayne Blvd Ste 1212Miami, FL 33132-2309 · (305) 203-4711

Phone(305) 203-4711

Organization SubpartNo

Authorized OfficialFrank GillenAuthorized Official · (214) 680-5000

Enumeration DateFebruary 26, 2021

Last NPPES UpdateMay 18, 20212 updates tracked since enumeration

NPPES CertifiedMay 18, 2021

✔ NPI 1760076061 is a valid, active identifier and passes the ISO check-digit test.

Specialties & Licenses 2

★ 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.

Also ListedPhysiological LaboratoryTaxonomy 293D00000X

100 BISCAYNE BLVD STE 1212, Miami, FL 33132

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CLIA Laboratory Certificates CMS CLIA

Laboratory certificates issued under the Clinical Laboratory Improvement Amendments (CLIA) program, which sets federal quality standards for human laboratory testing in the United States. There is no official CMS crosswalk between CLIA and NPI numbers; these certificates are associated with this NPI by matching facility names, locations and phone numbers in the CMS CLIA registry.

Certificate of Accreditation 10D2210020

Precheck Health Services, Inc · Miami, FL

Active · expires May 10, 2028

CLIA Number10D2210020

Laboratory TypeIndependent

Certificate Effective DateMay 11, 2026

Certificate Expiration DateMay 10, 2028

Laboratory DirectorDr. Lourdes M. Trigo

Laboratory Phone(214) 680-5000

Laboratory LocationPrecheck Health Services, Inc100 Biscayne Boulevard, Ste 1611, Miami, FL 33132

CLIA data matches this NPI record on: Name Phone

This is a certificate that is issued to a laboratory on the basis of the laboratory's accreditation by an accreditation organization approved by CMS.

Areas of Expertise CMS Part B claims 38

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 (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.

636 services634 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.

561 services554 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.

521 services520 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.

518 services517 patients

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.

509 services509 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.

470 services468 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.

466 services464 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.

463 services463 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.

458 services457 patients

Test for detecting genes associated with intellectual disability, genomic sequence analysis panel, at least 60 genes 81470

This is a genetic test that examines a minimum of 60 genes in your DNA. It's designed to identify potential genetic factors that might be linked to intellectual disabilities. The test involves analyzing the specific sequences of these genes to detect any abnormalities.

456 services456 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.

455 services455 patients

Gene analysis (bruton's tyrosine kinase) for common variants 81233

Gene analysis of Bruton's Tyrosine Kinase (BTK) for common variants is a test that examines your BTK gene. This gene plays a crucial role in the immune system. By studying it, we can identify any variations that might be linked to certain health conditions.

442 services442 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.

436 services436 patients

Genomic sequence analysis panel for severe inherited conditions with sequencing of 15 or more genes 81443

This procedure involves analyzing your genetic material to identify specific mutations that could cause severe inherited conditions. It examines 15 or more genes. The information can help in diagnosis, treatment planning, and understanding your risk for certain diseases.

382 services382 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.

351 services350 patients

Gene analysis panel for hereditary disorders of the peripheral nervous system 81448

A gene analysis panel for hereditary disorders of the peripheral nervous system is a test that checks for genetic mutations linked to certain nerve disorders. It helps identify if you have a higher risk of developing these conditions.

335 services335 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.

321 services321 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.

317 services317 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.

315 services315 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.

298 services298 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.

288 services288 patients

Gene analysis (glucose-6-phosphatase, catalytic subunit) common variants 81250

Gene analysis of glucose-6-phosphatase, catalytic subunit, common variants involves studying specific genes related to glucose metabolism. This helps understand if you're at risk of certain metabolic disorders. It's a non-invasive procedure, involving a simple blood or saliva sample.

273 services273 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.

246 services246 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.

246 services246 patients

Test for detecting genes 81440

A gene detection test is a medical procedure that identifies specific genes in your DNA. It helps to understand your genetic makeup and potential health risks. The process involves taking a small sample of your body tissue, like blood or saliva, which is then analyzed in a lab.

181 services181 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.

137 services137 patients

Gene analysis panel for evaluation of genes associated with epilepsy 81419

A gene analysis panel for epilepsy evaluates specific genes linked to this condition. This test can help understand your epilepsy type and severity, potentially guiding treatment options. It involves a blood sample and lab analysis.

124 services124 patients

Hla class i and ii typing low resolution hla-a, -b, -c, -drb1/3/4/5 and -dqb1 81370

HLA Class I and II typing is a lab test that identifies specific proteins on your cells. These proteins play a crucial role in your immune system's response to foreign substances. This test is often done before organ transplants to ensure compatibility.

123 services123 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.

84 services84 patients

Test for detecting genes associated with rheumatoid arthritis using immunoassay technique 81490

This procedure involves a blood test that uses an immunoassay technique to detect specific genes linked to rheumatoid arthritis. It helps identify your risk of developing the condition and can inform treatment strategies.

63 services63 patients

Test for detecting genes associated with intellectual disability, duplication/deletion gene analysis, at least 60 genes 81471

This test identifies changes in at least 60 genes linked to intellectual disability. It involves analyzing your DNA to find any duplications or deletions in these genes. This information can help in understanding and managing the condition.

62 services62 patients

Test for detecting genes associated with disease, whole mitochondrial genome 81465

A test for the whole mitochondrial genome identifies changes in the mitochondrial DNA that may cause health issues. It involves taking a small sample of blood or tissue. The DNA is then examined for any changes linked to potential diseases.

51 services51 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.

50 services50 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.

45 services45 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.

39 services39 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.

13 services13 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.

13 services13 patients

Gene analysis (udp glucuronosyltransferase 1 family, polypeptide a1) for detection of common variants 81350

Gene analysis for UDP glucuronosyltransferase 1 family, polypeptide A1 is a test that checks for common genetic variations. These variations can affect how your body processes certain substances, potentially impacting your health. Knowing your genetic makeup can help guide your healthcare.

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.

PRECHECK HEALTH SERVICES INC

Physiological Laboratory

100 BISCAYNE BLVD STE 1212
MIAMI, FL 33132

Miami-Dade County (305) 203-4711

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 Precheck Health Services Inc's NPI number?

The NPI number for Precheck Health Services Inc is 1760076061. It was assigned to this organization in the NPPES registry on February 26, 2021.

Where is Precheck Health Services Inc located?

Precheck Health Services Inc is located at 100 Biscayne Blvd Ste 1212, Miami, FL 33132. The listed phone number is (305) 203-4711.

What is Precheck Health Services Inc's specialty?

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

Does Precheck Health Services Inc hold a CLIA laboratory certificate?

Yes. A Certificate of Accreditation (number 10D2210020) is associated with this NPI, valid through May 10, 2028. CLIA certificates authorize laboratory testing under the federal Clinical Laboratory Improvement Amendments program.

When was this NPI record last updated?

The NPPES record for Precheck Health Services Inc was last updated on May 18, 2021. NPI Profile syncs with the weekly NPPES data releases published by CMS.