NEOGENOMICS LABORATORIES INC NPI 1396408829

NPI Details

NEOGENOMICS LABORATORIES INC is a clinical medical laboratory in Fort Myers, FL. 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 1396408829. The provider is registered as an organization entity type.

The provider's business location address is:

9490 NEOGENOMICS WAY
FORT MYERS, FL
ZIP 33912
Phone: (866) 776-5904
Fax: (888) 443-4153

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

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)
• Microscopic genetic analysis of tissue, computer-assisted technology, initial procedure, each multiplex procedure (HCPCS:88374)
• Translocation analysis (bcr/abl1) major breakpoint (HCPCS:81206)
• Special stained specimen slides to examine tissue, each additional procedure (HCPCS:88341)
• Tissue culture for tumor disorders of bone marrow and blood cells (HCPCS:88237)
• Microscopic genetic analysis of tissue, computer-assisted technology, initial procedure, each multiplex procedure (HCPCS:88374)
• Flow cytometry technique for dna or cell analysis, first marker (HCPCS:88184)
• Special stained specimen slides to examine tissue, each additional procedure (HCPCS:88341)
• Interpretation and report of genetic testing (HCPCS:88291)
• Translocation analysis (bcr/abl1) minor breakpoint (HCPCS:81207)
• Special stained specimen slides to examine tissue, initial procedure (HCPCS:88342)
• Special stained specimen slides to examine tissue including interpretation and report (HCPCS:88313)
• Microscopic genetic analysis of tumor, using computer-assisted technology (HCPCS:88361)
• Microscopic genetic analysis of tumor, manual (HCPCS:88360)
• Gene analysis (janus kinase 2) variant (HCPCS:81270)
• Microscopic genetic analysis of tumor, manual (HCPCS:88360)
• Test for detecting genes associated with cancer (HCPCS:81455)
• Flow cytometry technique for dna or cell analysis, 16 or more markers (HCPCS:88189)
• Special stained specimen slides to examine tissue, initial procedure (HCPCS:88342)
• Microscopic genetic analysis of tumor, using computer-assisted technology (HCPCS:88361)
• Gene analysis (janus kinase 2) targeted sequence analysis (HCPCS:81279)
• Special stained specimen slides to examine tissue including interpretation and report (HCPCS:88313)
• Pathology examination of tissue using a microscope, intermediate complexity (HCPCS:88305)
• Gene analysis (calreticulin), common variants (HCPCS:81219)
• Gene analysis (mpl proto-oncogene, thrombopoietin receptor) sequence analysis of exon 10 (HCPCS:81339)
• Chromosome analysis for genetic defects, analyze 20-25 cells (HCPCS:88264)
• Cell examination of urine, manual (HCPCS:88120)
• Test for detecting genes associated with blood related cancer (HCPCS:81450)
• Bone marrow, smear interpretation (HCPCS:85097)
• Preparation of tissue for examination by removing any calcium present (HCPCS:88311)
• Pathology examination of tissue using a microscope, intermediate complexity (HCPCS:88305)
• Gene analysis (v-raf murine sarcoma viral oncogene homolog b1) (HCPCS:81210)
• Gene rearrangement analysis detection abnormal clonal population (t cell antigen receptor gamma) (HCPCS:81342)
• Gene rearrangement analysis (immunoglobulin heavy chain locus), variable region somatic mutation analysis (HCPCS:81263)
• 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)
• Gene analysis (t cell antigen receptor beta) amplification methodology (HCPCS:81340)
• Gene analysis (myeloid differentiation primary response 88) for p.leu265pro variant (HCPCS:81305)
• Preparation of tissue for examination by removing any calcium present (HCPCS:88311)
• Genetic sequencing localization, initial procedure (HCPCS:88365)
• Genetic sequencing localization, each additional procedure (HCPCS:88364)
• Gene rearrangement analysis (immunoglobulin kappa light chain locus) to detect abnormal clonal population (HCPCS:81264)
• Gene rearrangement analysis (immunoglobulin heavy chain locus) to detect abnormal clonal population amplified methodology (HCPCS:81261)
• Gene analysis (epidermal growth factor receptor), common variants (HCPCS:81235)
• Gene analysis (tumor protein 53) targeted sequence analysis (HCPCS:81352)
• Surgical pathology consultation and report on referred slides prepared elsewhere (HCPCS:88321)
• Gene analysis (v-ki-ras2 kirsten rat sarcoma viral oncogene) variants in codons 12 and 13 (HCPCS:81275)
• Gene analysis (kirsten rat sarcoma viral oncogene homolog), additional variants (HCPCS:81276)
• Translocation analysis (bcr/abl1) other breakpoint (HCPCS:81208)
• Gene analysis (abl proto-oncogene 1, non-receptor tyrosine kinase) (HCPCS:81170)
• Genetic sequencing localization, initial procedure (HCPCS:88365)
• Surgical pathology consultation and report on referred material requiring preparation of slides (HCPCS:88323)
• Test for detecting genes associated with colon cancer, promoter methylation analysis (HCPCS:81288)
• Genetic sequencing localization, each additional procedure (HCPCS:88364)
• Microsatellite instability analysis (HCPCS:81301)
• Gene analysis (neurotrophic receptor tyrosine kinase 1, 2, and 3) translocation analysis (HCPCS:81194)
• Gene analysis (v-kit hardy-zuckerman 4 feline sarcoma viral oncogene homolog), targeted sequence (HCPCS:81272)
• Cell examination of urine, computer-assisted (HCPCS:88121)
• Test for detecting genes associated with cancer of body organ (HCPCS:81445)
• Translocation analysis (pml-rara regulated adaptor molecule 1) common breakpoint (HCPCS:81315)
• Special stained specimen slides to examine tissue, each multiplex procedure (HCPCS:88344)
• Gene analysis (fms-related tyrosine kinase 3) internal tandem duplication variants (HCPCS:81245)
• Test for detecting genes associated with blood cancer (HCPCS:81246)
• Gene analysis for cancer (neuroblastoma) (HCPCS:81311)
• Microscopic genetic analysis of tissue, computer-assisted technology, initial procedure (HCPCS:88367)
• Flow cytometry technique for dna or cell analysis, 9 to 15 markers (HCPCS:88188)
• Gene analysis (isocitrate dehydrogenase 1 [nadp+], soluble) for common variants (HCPCS:81120)
• Gene analysis (isocitrate dehydrogenase 2 [nadp+], mitochondrial) for common variants (HCPCS:81121)
• Blood smear interpretation by physician with written report (HCPCS:85060)
• Gene analysis (nucleophosmin) exon 12 variants (HCPCS:81310)
• Gene analysis (splicing factor [3b] subunit b1) for detection of common variants (HCPCS:81347)
• Flow cytometry technique for dna or cell analysis, 2 to 8 markers (HCPCS:88187)
• 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 (ccnd1/igh (t(11;14))) translocation analysis (HCPCS:81168)

The enumeration date for this NPI number is 10/21/2021 and was last updated on 12/9/2024.

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: