ELITE CLINICAL LABORATORY, INC
NPI 1215055256
Clinical Medical Laboratory in Houston, TX

Q: What is Elite Clinical Laboratory, Inc's NPI number?

The NPI number for Elite Clinical Laboratory, Inc is 1215055256. It was assigned to this organization in the NPPES registry on March 27, 2007.

Q: What is Elite Clinical Laboratory, Inc's specialty?

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

Active since March 27, 2007

3600 S GESSNER RD STE 110, HOUSTON, TX 77063(281) 617-7586 Get Directions Write a Review

NPPES record last updated: August 10, 2023. Verified against the NPPES registry weekly; last sync: August 16, 2026.

Record update history: Aug 10, 2023, Apr 27, 2022, Mar 25, 2020 and 1 more (4 updates tracked since 2019).

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About Elite Clinical Laboratory, Inc NPPES

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

ELITE CLINICAL LABORATORY, INC (NPI 1215055256) is a healthcare organization registered as a clinical medical laboratory in Houston, Texas and active in the NPI registry since March 2007. The organization lists Chad Harper, Owner, as its authorized official.

NPPES Registry Identity

NPI1215055256

Entity TypeOrganization

Primary Taxonomy291U00000X

Legal Business NameELITE CLINICAL LABORATORY, INC

Location Address3600 S GESSNER RD STE 110Houston, TX 77063-5149

Mailing Address3600 S Gessner Rd Ste 110Houston, TX 77063-5149 · (281) 617-7586

Phone(281) 617-7586

Organization SubpartNo

Authorized OfficialChad HarperOwner · (832) 316-7764

Enumeration DateMarch 27, 2007

Last NPPES UpdateAugust 10, 20234 updates tracked since enumeration

NPPES CertifiedAugust 10, 2023

✔ NPI 1215055256 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.

3600 S GESSNER RD STE 110, Houston, TX 77063

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Areas of Expertise CMS Part B claims 61

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.

Testing for presence of drug, by chemistry analyzers 80307

Chemistry analyzers are used to detect the presence of drugs in your system. This test involves taking a small sample of your blood or urine. The sample is then analyzed for specific substances. The results help in understanding your health condition better.

2,443 services1,142 patients

Drug test(s), definitive, utilizing (1) drug identification methods able to identify individual drugs and distinguish between structural isomers (but not necessarily stereoisomers), including, but not limited to gc/ms (any type, single or tandem) and lc/ms G0482

A definitive drug test identifies specific drugs in your system. Advanced methods like GC/MS (Gas Chromatography/Mass Spectrometry) and LC/MS (Liquid Chromatography/Mass Spectrometry) are used. These can distinguish between similar drugs, providing precise results.

1,798 services1,125 patients

A definitive drug test identifies specific drugs in your system. It uses advanced methods like gc/ms and lc/ms, which can distinguish between different types of drugs but not necessarily their 3D forms. This test offers detailed results to support your healthcare decisions.

1,682 services1,258 patients

Detection test by nucleic acid for organism, amplified probe technique 87798

A nucleic acid detection test is a procedure to identify specific organisms in your body. This test uses an amplified probe technique, which magnifies the genetic material of the organism, making it easier to detect. It's a precise way to diagnose infections.

841 services68 patients

Molecular pathology procedure level 1 81400

A Molecular Pathology Procedure Level 1 is a lab test that studies the genes in your cells. It helps identify alterations in your DNA that may cause or contribute to certain diseases. The procedure is non-invasive and helps in early disease detection.

764 services481 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.

459 services459 patients

Gene analysis (cytochrome p450, family 2, subfamily d, polypeptide 6) common variants 81226

Gene analysis of cytochrome P450 2D6 (CYP2D6) common variants involves studying specific genes to understand your body's ability to process certain medications. This can help tailor treatments to your unique genetic makeup, optimizing medication effectiveness and safety.

354 services354 patients

Fetal congenital abnormalities, biochemical assays of two proteins (papp-a, hcg [any form]), utilizing maternal serum, algorithm reported as a risk score 81508

This test examines two proteins in a mother's blood to detect potential irregularities in the unborn baby's development. The results, combined with other factors, provide a risk score that helps assess the likelihood of certain conditions.

328 services328 patients

Gene analysis (retinal disorders), genomic sequence 81434

Gene analysis for retinal disorders is a process where your DNA is examined to identify any changes or mutations that may be causing or could lead to vision problems. It's like reading a book to find any spelling mistakes that could alter the story.

325 services325 patients

Test for detecting genes causing hearing loss genomic sequence analysis panel, at least 60 genes 81430

This is a genetic test that examines at least 60 different genes to identify any changes linked to hearing loss. By studying your DNA, the test can help determine if you have genes that may cause hearing loss, aiding in diagnosis and treatment planning.

318 services318 patients

Gene analysis (gap junction protein, beta 6, 30kda, connexin 30), common variants 81254

Gene analysis for Connexin 30 involves studying your DNA to identify variations in the GJB6 gene. This gene helps produce a protein vital for cell communication. Detecting common variants can help understand certain health conditions.

316 services316 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.

308 services308 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.

303 services303 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.

301 services301 patients

Gene analysis (transforming growth factor beta-induced) for common variants 81333

Gene analysis for common variants in the transforming growth factor beta-induced (TGFBI) gene helps understand your genetic makeup better. This procedure checks for variations in the TGFBI gene, which can influence your health. It's a safe, non-invasive test that uses a simple blood or saliva sample.

275 services275 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.

250 services250 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.

243 services243 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.

210 services210 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.

189 services189 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.

183 services183 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.

180 services180 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.

161 services161 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.

156 services156 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.

156 services156 patients

Detection test for candida species (yeast), amplified probe technique 87481

This test helps identify Candida, a type of fungus often present in the human body. An amplified probe technique is used, which enhances detection of the fungus in a sample. This method increases the accuracy of the test, helping to determine the best treatment.

155 services69 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.

146 services146 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.

141 services141 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.

141 services141 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.

136 services136 patients

Gene analysis (aspartoacylase) 81200

Gene analysis for aspartoacylase is a test that studies your DNA to check for mutations in the ASPA gene. This gene is responsible for producing an enzyme called aspartoacylase, which plays a crucial role in brain development and function. Any changes could lead to health issues.

116 services116 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.

116 services116 patients

Gene analysis (glucosidase, beta, acid) common variants 81251

Gene analysis of common variants in the beta-glucosidase acid enzyme helps understand certain health conditions. This enzyme plays a key role in the body's metabolism. By studying its variants, doctors can better diagnose and treat metabolic disorders.

113 services113 patients

Gene analysis (hemochromatosis) common variants 81256

Gene analysis for hemochromatosis common variants is a test that checks for specific changes in your DNA. These changes could indicate a higher risk of developing hemochromatosis, a condition that causes your body to absorb too much iron from your diet.

110 services110 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.

109 services109 patients

Gene analysis (sphingomyelin phosphodiesterase 1, acid lysosomal) common variants 81330

Gene analysis of sphingomyelin phosphodiesterase 1, acid lysosomal, involves studying specific variants in your genes. This helps understand your body's enzyme production, which can influence health conditions. It's a non-invasive procedure using a simple blood or saliva sample.

103 services103 patients

Gene analysis (serpin peptidase inhibitor, clade a, alpha-1 antiproteinase, antitrypsin, member 1) common variants 81332

Gene analysis for SERPINA1 common variants is a test that checks for changes in the SERPINA1 gene. This gene helps protect your lungs and liver from damage. Certain changes can lead to conditions like lung disease or liver problems. This test helps identify those changes.

103 services103 patients

Gene analysis (cytochrome p450, family 2, subfamily c, polypeptide 9) common variants 81227

Gene analysis for cytochrome P450 2C9 common variants is a test to identify specific genetic variations. These variations can affect how your body processes certain medications, helping to determine the most effective and safe drug dosage for you.

91 services91 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.

89 services89 patients

Detection test by nucleic acid for staphylococcus aureus (bacteria), amplified probe technique 87640

A detection test for Staphylococcus aureus uses a method called the amplified probe technique. This method identifies the bacteria's unique genetic material, or nucleic acid, helping to confirm its presence. It's a highly accurate way to detect this type of bacteria.

75 services68 patients

Detection test by nucleic acid for strep (streptococcus, group a), amplified probe technique 87651

This test detects Group A Streptococcus bacteria in your body. It uses an amplified probe technique, which amplifies the bacteria's nucleic acid, making it easier to identify. This test helps diagnose conditions like strep throat or scarlet fever.

75 services68 patients

Detection test by nucleic acid for strep (streptococcus, group b), amplified probe technique 87653

A detection test by nucleic acid for Group B Strep uses an amplified probe technique. This test identifies the presence of Group B Strep bacteria in the body. It involves collecting a sample, usually a swab, which is then examined in a lab for the bacteria's genetic material.

64 services59 patients

Identification of organisms by genetic analysis, amplified probe technique 87150

This procedure involves identifying organisms like bacteria or viruses in your body. It's done by amplifying a small part of their genetic material, making it easier to detect. This technique helps in accurate diagnosis and appropriate treatment.

60 services25 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.

54 services54 patients

Quantitative measurement of severe acute respiratory syndrome coronavirus 2 (covid-19] antibody 86413

This procedure measures the level of COVID-19 antibodies in your body. It involves taking a blood sample, which is then tested in a lab. The results can indicate if you've had a past infection. However, it doesn't confirm immunity or protection against future infection.

44 services40 patients

Detection test by nucleic acid for chlamydia pneumoniae, amplified probe technique 87486

This test checks for the presence of Chlamydia pneumoniae, a bacterium that can cause respiratory infections. It uses an amplified probe technique, which magnifies the bacterium's genetic material for easier detection. It's a standard, non-invasive procedure.

44 services40 patients

Detection test by nucleic acid for cytomegalovirus (cmv), amplified probe technique 87496

A detection test by nucleic acid for cytomegalovirus (CMV) using an amplified probe technique is a lab procedure. It identifies the presence of CMV, a common virus, in your body. This technique amplifies the virus's genetic material, making it easier to detect.

44 services40 patients

Detection test by nucleic acid for enterovirus (intestinal virus), amplified probe technique 87498

This test identifies the presence of an enterovirus, a type of virus that primarily targets the digestive system. It uses a method called the amplified probe technique to boost the detection of the virus's genetic material, or nucleic acid.

44 services40 patients

Detection test by nucleic acid for multiple types influenza virus 87502

A detection test by nucleic acid for multiple types of influenza virus is a diagnostic procedure. It identifies the genetic material of the virus in your body. It's highly accurate and can distinguish between different flu strains, helping in prompt and precise treatment.

44 services40 patients

Detection test by nucleic acid for multiple types influenza virus, each additional influenza virus type or sub-type 87503

This test identifies various types of influenza viruses by analyzing their genetic material, or nucleic acid. It can detect multiple flu types or sub-types, providing a more precise diagnosis to aid in appropriate treatment.

44 services40 patients

Detection test by nucleic acid for herpes virus-6, amplified probe technique 87532

A detection test by nucleic acid for herpes virus-6, amplified probe technique, is a lab procedure that identifies the presence of herpes virus-6 in your body. It does this by amplifying and detecting the virus's genetic material, aiding in accurate diagnosis and treatment planning.

44 services40 patients

Detection test by nucleic acid for legionella pneumophila (water borne bacteria), amplified probe technique 87541

A detection test for Legionella Pneumophila, a waterborne bacteria, uses the amplified probe technique. This involves identifying the bacteria's unique genetic material (nucleic acid) and amplifying it for easier detection, aiding in accurate diagnosis.

44 services40 patients

Detection test by nucleic acid for mycobacteria tuberculosis (tb bacteria), amplified probe technique 87556

A detection test by nucleic acid for Mycobacteria Tuberculosis, using an amplified probe technique, is a diagnostic test for TB. It identifies the TB bacteria's genetic material in your body. It's fast, highly accurate, and can confirm TB presence even in small samples.

44 services40 patients

Detection test by nucleic acid for mycoplasma pneumoniae (bacteria), amplified probe technique 87581

This test checks for Mycoplasma pneumoniae, a bacteria that can cause lung infection. It uses a method called amplified probe technique, which identifies the bacteria's genetic material. This helps in diagnosing the infection accurately.

44 services40 patients

Detection test by nucleic acid for multiple types of respiratory virus, multiple types or subtypes, 3-5 targets 87631

This test identifies different respiratory viruses by examining their nucleic acid, the building blocks of their genetic material. It can detect multiple types or subtypes, specifically 3-5 targets. This helps in diagnosing your respiratory illness accurately.

44 services40 patients

Detection test by nucleic acid for respiratory syncytial virus, amplified probe technique 87634

This test identifies the presence of the Respiratory Syncytial Virus (RSV) in your body. It uses a technique called the amplified probe, which increases the amount of viral genetic material, making it easier to detect. This helps in diagnosing RSV infections accurately.

44 services40 patients

Detection test by nucleic acid for vancomycin resistance strep (vre), amplified probe technique 87500

The detection test by nucleic acid for vancomycin-resistant strep (VRE) is a laboratory procedure. It uses an amplified probe technique to identify specific genetic material in bacteria. This helps determine if the bacteria are resistant to the antibiotic vancomycin.

32 services29 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.

31 services31 patients

Detection test by nucleic acid for staphylococcus aureus, methicillin resistant (mrsa bacteria), amplified probe technique 87641

A detection test by nucleic acid for MRSA bacteria uses an amplified probe technique. It's a lab procedure that identifies the presence of MRSA, a type of bacteria resistant to many antibiotics. This test helps in deciding the best treatment.

29 services26 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.

25 services25 patients

Gene analysis (adenomatous polyposis coli), duplication or deletion variants 81203

Gene analysis of the adenomatous polyposis coli is a test that detects changes in the APC gene. These changes may cause certain health conditions. Duplication or deletion variants refer to parts of the gene being repeated or missing. This information helps tailor treatment plans.

20 services20 patients

Gene analysis (muts homolog 2, colon cancer, nonpolyposis type 1) duplication or deletion variants 81297

Gene analysis for MUTS homolog 2 (colon cancer, nonpolyposis type 1) duplication or deletion variants is a test that looks for changes in a specific gene linked to a higher risk of colon cancer. It helps identify if you carry these gene changes, aiding in early detection and prevention.

20 services20 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.

ELITE CLINICAL LABORATORY, LLC

Clinical Medical Laboratory

3600 S GESSNER RD STE 110
HOUSTON, TX 77063

Harris County (281) 795-5603

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 Elite Clinical Laboratory, Inc's NPI number?

The NPI number for Elite Clinical Laboratory, Inc is 1215055256. It was assigned to this organization in the NPPES registry on March 27, 2007.

Where is Elite Clinical Laboratory, Inc located?

Elite Clinical Laboratory, Inc is located at 3600 S Gessner Rd Ste 110, Houston, TX 77063. The listed phone number is (281) 617-7586.

What is Elite Clinical Laboratory, Inc'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 Elite Clinical Laboratory, Inc was last updated on August 10, 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.