CARE VIEW DIAGNOSTICS LLC
NPI 1093582850
Clinical Medical Laboratory in Dallas, TX

Q: What is Care View Diagnostics LLC's NPI number?

The NPI number for Care View Diagnostics LLC is 1093582850. It was assigned to this organization in the NPPES registry on December 11, 2023.

Q: What is Care View Diagnostics LLC's specialty?

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

Active since December 11, 2023

16990 DALLAS PKWY STE 101, DALLAS, TX 75248(469) 361-2622(469) 868-4302 Get Directions Write a Review

NPPES record last updated: January 18, 2024. Verified against the NPPES registry weekly; last sync: August 09, 2026.

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About Care View Diagnostics Llc NPPES

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

CARE VIEW DIAGNOSTICS LLC (NPI 1093582850) is a healthcare organization registered as a clinical medical laboratory in Dallas, Texas and active in the NPI registry since December 2023. The organization lists Mohammed M Aldalki, Authorized Official, as its authorized official.

NPPES Registry Identity

NPI1093582850

Entity TypeOrganization

Primary Taxonomy291U00000X

Legal Business NameCARE VIEW DIAGNOSTICS LLC

Location Address16990 DALLAS PKWY STE 101Dallas, TX 75248-1998

Mailing Address16990 Dallas Pkwy Ste 101Dallas, TX 75248-1998 · (469) 361-2622 · Fax (469) 868-4302

Phone(469) 361-2622

Fax(469) 868-4302

Organization SubpartNo

Authorized OfficialMohammed M AldalkiAuthorized Official · (469) 361-2622

Enumeration DateDecember 11, 2023

Last NPPES UpdateJanuary 18, 2024

NPPES CertifiedJanuary 18, 2024

✔ NPI 1093582850 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.

16990 DALLAS PKWY STE 101, Dallas, TX 75248

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Areas of Expertise CMS Part B claims 15

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.

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.

1,407 services1,407 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.

1,407 services1,407 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.

1,407 services1,407 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.

1,392 services1,392 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.

360 services360 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.

360 services360 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.

354 services354 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.

352 services352 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.

348 services348 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.

348 services348 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.

348 services348 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.

347 services347 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.

347 services347 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.

347 services347 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.

334 services334 patients

Frequently Asked Questions NPPES & CMS

Common questions about this NPI record, answered from the official NPPES registry and CMS datasets shown on this page.

What is Care View Diagnostics LLC's NPI number?

The NPI number for Care View Diagnostics LLC is 1093582850. It was assigned to this organization in the NPPES registry on December 11, 2023.

Where is Care View Diagnostics LLC located?

Care View Diagnostics LLC is located at 16990 Dallas Pkwy Ste 101, Dallas, TX 75248. The listed phone number is (469) 361-2622.

What is Care View 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 Care View Diagnostics LLC was last updated on January 18, 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.