Data / Medical devices / Colorimeter, Photometer, Spectrophotometer For Clinical Use / United States
FDA-registered makers of Colorimeter, Photometer, Spectrophotometer For Clinical Use in the United States: 34 establishments
34 establishments in the United States are registered with the FDA to make Colorimeter, Photometer, Spectrophotometer For Clinical Use (product code JJQ). 5 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 3, 2026.
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- Device
- Colorimeter, Photometer, Spectrophotometer For Clinical Use
- Product code
- JJQ
- Country
- United States
Makers of Colorimeter, Photometer, Spectrophotometer For Clinical Use in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Teco Diagnostics | Anaheim, CA, United States | Manufacturer | 2 | March 1, 1990 | 0 | 0 | 0 | api.fda.gov |
| Beckman Coulter, Inc. | West Sacramento, CA, United States | Specification developer | 1 | March 17, 1980 | 0 | 1 | 0 | api.fda.gov |
| Diagnostic Automation/ Cortez Diagnostics Inc,. | Woodland Hills, CA, United States | Manufacturer | 1 | March 1, 1990 | 0 | 0 | 0 | api.fda.gov |
| Hologic, Inc. | San Diego, CA, United States | Manufacturer | 1 | January 23, 1991 | 0 | 0 | 0 | api.fda.gov |
| Siemens Healthcare Diagnostics Inc. | Newark, DE, United States | Manufacturer | 1 | January 11, 1991 | 0 | 0 | 0 | api.fda.gov |
| Associates Of Cape Cod, Inc. | E Falmouth, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Astoria-Pacific, Inc. | Clackamas, OR, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Awareness Technology, Inc. | Palm City, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Advanced Instruments, LLC | Westbrook, ME, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Agilent Technologies, Inc | Santa Clara, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Agilent Technologies, Inc. | Winooski, VT, United States | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Ameditech, Inc. | San Diego, CA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Applied BioCode, Inc. | Santa Fe Springs, CA, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Baebies Inc. | Durham, NC, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beckman Coulter, Inc. | Miami, FL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Becton, Dickinson & Co. | Sparks, MD, United States | Complaint file establishment, Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Chembio Diagnostic Systems, Inc. | Medford, NY, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Codonics, Inc. | Middleburg Heights, OH, United States | Complaint file establishment, Manufacturer, Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Diasorin Inc. | Stillwater, MN, United States | Manufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Dynex Technologies, Inc. | Chantilly, VA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Healgen Scientific LLC | Houston, TX, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hemagen Diagnostics, Inc. | Baltimore, MD, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| High Technology, Inc. | North Attleboro, MA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Immunocentrix Corporation | Canoga Park, CA, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| IMMY, Inc. | Norman, OK, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Logic PD, Inc. | Eden Prairie, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medtox Diagnostics, Inc. | Burlington, NC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medtox Diagnostics, Inc. | Burlington, NC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Monobind, Inc. | Lake Forest, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Princeton Biomeditech Corp. | Monmouth Jct, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Princeton BioMeditech Corp. | Plainsboro, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Princeton BioMeditech Corp. | Skillman, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Qualigen, Inc. | Carlsbad, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vigilant Biosciences Inc. | Lakeway, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.