Data / Medical devices / Test, Cannabinoid, Employment And Insurance Testing, Exempt / United States
FDA-registered makers of Test, Cannabinoid, Employment And Insurance Testing, Exempt in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Test, Cannabinoid, Employment And Insurance Testing, Exempt (product code PVJ). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Test, Cannabinoid, Employment And Insurance Testing, Exempt
- Product code
- PVJ
- Country
- United States
Makers of Test, Cannabinoid, Employment And Insurance Testing, Exempt in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Advin Biotech, Inc. | San Diego, CA, United States | Contract manufacturer, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alere San Diego, Inc. | Pomona, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ameditech, Inc. | San Diego, CA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Chemtron Biotech, Inc. | San Diego, CA, United States | Complaint file establishment, Contract manufacturer, 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 | |
| Labone, Inc. | Lenexa, KS, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mlife Diagnostics LLC | Marshall, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Orfila Diagnostics Inc. Dba Nform | Wilmington, DE, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Premier Biotech, LLC | Minneapolis, MN, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| W.H.P.M., Inc. | Irwindale, CA, United States | Contract 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.