NPI Details
NEOGENOMICS LABORATORIES INC is a clinical medical laboratory in Ramsey, NJ. 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 1205063294. The provider is registered as an organization entity type.
The provider .
The provider's business location address is:
535 E CRESCENT AVE
RAMSEY, NJ
ZIP 07446-922
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 (513) 607-7872.
The CLIA number assigned to this NPI record is 31D2050001 - 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)
- Pathology examination of tissue using a microscope, intermediate complexity (HCPCS:88305)
- Infectious agent detection by nucleic acid (dna or rna); severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19]), amplified probe technique, making use of high throughput technologies as described by cms-2020-01-r (HCPCS:U0003)
- Infectious agent detection by nucleic acid (dna or rna); severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19]), amplified probe technique, cdc or non-cdc, making use of high throughput technologies, completed within (HCPCS:U0005)
- Special stained specimen slides to examine tissue, each additional procedure (HCPCS:88341)
- Microscopic genetic analysis of tissue, manual, each additional multiplex stain procedure (HCPCS:88377)
- 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, manual (HCPCS:88360)
- Flow cytometry technique for dna or cell analysis, 16 or more markers (HCPCS:88189)
- Flow cytometry technique for dna or cell analysis, first marker (HCPCS:88184)
- Preparation of tissue for examination by removing any calcium present (HCPCS:88311)
- Test for detecting genes associated with blood related cancer (HCPCS:81450)
- Microscopic genetic analysis of tissue, manual, initial procedure (HCPCS:88368)
- Cell examination of specimen, selective cellular enhancement technique (HCPCS:88112)
- Molecular pathology procedure; physician interpretation and report (HCPCS:G0452)
- Bone marrow, smear interpretation (HCPCS:85097)
- Genetic sequencing localization, initial procedure (HCPCS:88365)
- Pathology examination of tissue using a microscope, moderately low complexity (HCPCS:88304)
- Tissue culture for tumor disorders of bone marrow and blood cells (HCPCS:88237)
- Genetic sequencing localization, each additional procedure (HCPCS:88364)
- Special stained specimen slides to identify organisms including interpretation and report (HCPCS:88312)
- Detection test by multiplex amplified probe technique for severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (covid-19) and influenza virus types a and b (HCPCS:87636)
- Chromosome analysis for genetic defects, additional karyotypes, each study (HCPCS:88280)
- Cell examination of urine, manual (HCPCS:88120)
- Chromosome analysis for genetic defects, count 15-20 cells (HCPCS:88262)
- Translocation analysis (bcr/abl1) major breakpoint (HCPCS:81206)
- Translocation analysis (bcr/abl1) minor breakpoint (HCPCS:81207)
- Gene analysis (janus kinase 2) variant (HCPCS:81270)
- Preparation of specimen, manual (HCPCS:88381)
- Gene analysis (janus kinase 2) targeted sequence analysis (HCPCS:81279)
- Pathology examination of tissue using a microscope, moderately high complexity (HCPCS:88307)
- Gene rearrangement analysis (immunoglobulin heavy chain locus), variable region somatic mutation analysis (HCPCS:81263)
- Chromosome analysis for genetic defects, additional cells counted, each study (HCPCS:88285)
- Pap test, automated thin layer preparation; automated system and manual rescreening (HCPCS:88175)
- Gene analysis (mpl proto-oncogene, thrombopoietin receptor) sequence analysis of exon 10 (HCPCS:81339)
- Test for detecting genes associated with blood cancer (HCPCS:81246)
- Gene analysis (fms-related tyrosine kinase 3) internal tandem duplication variants (HCPCS:81245)
- Gene analysis (calreticulin), common variants (HCPCS:81219)
- Detection test by nucleic acid for human papillomavirus (hpv), high-risk types (HCPCS:87624)
- Surgical pathology consultation and report on referred material requiring preparation of slides (HCPCS:88323)
- Cell examination of specimen, concentration technique (HCPCS:88108)
- Test for detecting genes associated with cancer of body organ (HCPCS:81445)
- Chromosome analysis for genetic defects, count 5 cells (HCPCS:88261)
- Flow cytometry technique for dna or cell analysis, 2 to 8 markers (HCPCS:88187)
- Evaluation of fine needle aspirate with interpretation and report (HCPCS:88173)
- Gene analysis (abl proto-oncogene 1, non-receptor tyrosine kinase) (HCPCS:81170)
- Surgical pathology, gross and microscopic examinations, for prostate needle biopsy, any method (HCPCS:G0416)
The enumeration date for this NPI number is 6/17/2009 and was last updated on 10/3/2025.
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:
| No. |
Taxonomy Code |
Taxonomy Clasification |
Taxonomy Specialization |
License Number |
License State |
Primary |
| 1 | 291U00000X | Clinical Medical Laboratory | | | | Yes |