NEOGENOMICS LABORATORIES INC NPI 1447437355

NPI Details

NEOGENOMICS LABORATORIES INC is a clinical medical laboratory in Aliso Viejo, CA. The provider is (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. NEOGENOMICS LABORATORIES INC NPI is 1447437355. The provider is registered as an organization entity type.

The provider's business location address is:

31 COLUMBIA
ALISO VIEJO, CA
ZIP 92656
Phone: (866) 776-5907
Fax: (888) 443-4153

The provider's authorized official is Jeffrey Scott Sherman .
The authorized official title is Chief Financial Officer and has the following contact phone number (866) 776-5907.

The CLIA number assigned to this NPI record is 05D1021650 - independent with a certificate type of Certificate of Accreditation.

The following top HCPCS codes were publicly reported for this provider under the Medicare program for the year 2016. The reported codes are based on the top codes for each available Medicare specialty, excluding evaluation and management codes.

• Flow cytometry technique for dna or cell analysis, each additional marker (HCPCS:88185)
• Special stained specimen slides to examine tissue, each additional procedure (HCPCS:88341)
• Microscopic genetic analysis of tissue, computer-assisted technology, initial procedure, each multiplex procedure (HCPCS:88374)
• Microscopic genetic analysis of tissue, computer-assisted technology, initial procedure, each multiplex procedure (HCPCS:88374)
• Special stained specimen slides to examine tissue, each additional procedure (HCPCS:88341)
• Special stained specimen slides to examine tissue, initial procedure (HCPCS:88342)
• Interpretation and report of genetic testing (HCPCS:88291)
• Molecular pathology procedure (HCPCS:81479)
• Microscopic genetic analysis of tumor, manual (HCPCS:88360)
• Special stained specimen slides to examine tissue including interpretation and report (HCPCS:88313)
• Microscopic genetic analysis of tumor, manual (HCPCS:88360)
• Microscopic genetic analysis of tissue, manual, each additional multiplex stain procedure (HCPCS:88377)
• Microscopic genetic analysis of tissue, manual, each additional multiplex stain procedure (HCPCS:88377)
• Flow cytometry technique for dna or cell analysis, 16 or more markers (HCPCS:88189)
• Microscopic genetic analysis of tumor, using computer-assisted technology (HCPCS:88361)
• Microscopic genetic analysis of tumor, using computer-assisted technology (HCPCS:88361)
• Tissue culture for tumor disorders of bone marrow and blood cells (HCPCS:88237)
• Test for detecting genes associated with blood related cancer (HCPCS:81450)
• Flow cytometry technique for dna or cell analysis, first marker (HCPCS:88184)
• Special stained specimen slides to examine tissue, initial procedure (HCPCS:88342)
• Pathology examination of tissue using a microscope, intermediate complexity (HCPCS:88305)
• Translocation analysis (bcr/abl1) major breakpoint (HCPCS:81206)
• Gene analysis (janus kinase 2) variant (HCPCS:81270)
• Preparation of tissue for examination by removing any calcium present (HCPCS:88311)
• Chromosome analysis for genetic defects, analyze 20-25 cells (HCPCS:88264)
• Surgical pathology consultation and report on referred material requiring preparation of slides (HCPCS:88323)
• Genetic sequencing localization, initial procedure (HCPCS:88365)
• Genetic sequencing localization, each additional procedure (HCPCS:88364)
• Gene analysis (v-raf murine sarcoma viral oncogene homolog b1) (HCPCS:81210)
• Gene analysis (janus kinase 2) targeted sequence analysis (HCPCS:81279)
• Gene rearrangement analysis detection abnormal clonal population (t cell antigen receptor gamma) (HCPCS:81342)
• Gene analysis (calreticulin), common variants (HCPCS:81219)
• Special stained specimen slides to examine tissue including interpretation and report (HCPCS:88313)
• Gene analysis (mpl proto-oncogene, thrombopoietin receptor) sequence analysis of exon 10 (HCPCS:81339)
• Gene analysis (t cell antigen receptor beta) amplification methodology (HCPCS:81340)
• Gene analysis (myeloid differentiation primary response 88) for p.leu265pro variant (HCPCS:81305)
• Gene analysis (epidermal growth factor receptor), common variants (HCPCS:81235)
• Genetic sequencing localization, initial procedure (HCPCS:88365)
• Gene rearrangement analysis (immunoglobulin heavy chain locus), variable region somatic mutation analysis (HCPCS:81263)
• Bone marrow, smear interpretation (HCPCS:85097)
• Genetic sequencing localization, each additional procedure (HCPCS:88364)
• Test for detecting genes associated with colon cancer, promoter methylation analysis (HCPCS:81288)
• Test for detecting genes associated with cancer of body organ (HCPCS:81445)
• Microsatellite instability analysis (HCPCS:81301)
• Pathology examination of tissue using a microscope, intermediate complexity (HCPCS:88305)
• Gene analysis (abl proto-oncogene 1, non-receptor tyrosine kinase) (HCPCS:81170)
• Translocation analysis (bcr/abl1) other breakpoint (HCPCS:81208)
• Surgical pathology consultation and report on referred slides prepared elsewhere (HCPCS:88321)
• Gene analysis (v-kit hardy-zuckerman 4 feline sarcoma viral oncogene homolog), targeted sequence (HCPCS:81272)
• Special stained specimen slides to identify organisms including interpretation and report (HCPCS:88312)
• Cell examination of urine, manual (HCPCS:88120)
• Special stained specimen slides to examine tissue, each multiplex procedure (HCPCS:88344)
• Flow cytometry technique for dna or cell analysis, 9 to 15 markers (HCPCS:88188)
• Preparation of tissue for examination by removing any calcium present (HCPCS:88311)
• Gene analysis (nucleophosmin) exon 12 variants (HCPCS:81310)
• Translocation analysis (bcr/abl1) minor breakpoint (HCPCS:81207)
• Translocation analysis (pml-rara regulated adaptor molecule 1) common breakpoint (HCPCS:81315)
• Flow cytometry technique for dna or cell analysis, 2 to 8 markers (HCPCS:88187)
• Detection test by nucleic acid for human papillomavirus (hpv), high-risk types (HCPCS:87624)
• Special stained specimen slides to identify organisms including interpretation and report (HCPCS:88312)
• Gene analysis (o-6-methylguanine-dna methyltransferase) for promoter methylation (HCPCS:81287)
• Gene analysis (ccaat/enhancer binding protein [c/ebp], alpha) full gene sequence (HCPCS:81218)
• Gene analysis ((platelet-derived growth factor receptor, alpha polypeptide) targeted sequence (HCPCS:81314)
• Interpretation and report of genetic testing (HCPCS:88291)
• Cell examination of urine, manual (HCPCS:88120)
• Molecular pathology procedure level 2 (HCPCS:81401)
• Gene analysis (ccnd1/igh (t(11;14))) translocation analysis (HCPCS:81168)
• Blood smear interpretation by physician with written report (HCPCS:85060)
• Gene analysis (igh@/bcl2 (t(14;18)) translocation analysis (HCPCS:81278)
• Cell examination of urine, computer-assisted (HCPCS:88121)
• Flow cytometry technique for dna or cell analysis, 16 or more markers (HCPCS:88189)
• Gene analysis (breast cancer 1 and 2) of full sequence (HCPCS:81163)
• Microscopic genetic analysis of tissue, computer-assisted technology, initial procedure (HCPCS:88367)
• Tissue culture for tumor disorders of bone marrow and blood cells (HCPCS:88237)
• Microscopic genetic analysis of tissue, computer-assisted technology, initial procedure (HCPCS:88367)
• Gene analysis (partner and localizer of brca2) targeted sequence analysis (HCPCS:81309)
• Special stained specimen slides to examine tissue, each multiplex procedure (HCPCS:88344)
• Chromosome analysis for genetic defects, analyze 20-25 cells (HCPCS:88264)
• Blood smear interpretation by physician with written report (HCPCS:85060)

The enumeration date for this NPI number is 1/23/2008 and was last updated on 11/14/2024.

Taxonomy Codes

The NPI record includes the healthcare provider taxonomy classification, state license number and state of licensure. The following information regarding the scope of practice of this provider is available:

Other Identifiers

The following information regarding additional identifiers associated to this NPI record includes the other identifier number, identifier type, identifier state and issuer.