Contract manufacturerGEMINI BIOPRODUCTS LLC (West Sacramento, CA)CaliforniaHematologyClass I
GEMINI BIOPRODUCTS LLC
Contract manufacturer ยท West Sacramento, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3006236690 (openFDA record; or search FDA's registration database)
- FEI number
- 3006236690
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer; Repackager or relabeler
- Owner or operator
- Gemini Bioproducts LLC (FDA owner/operator no. 10058502)
- Registered address
- 920 Stillwater Road, Suite 130, West Sacramento, CA 95605
- Contract listings
- 3 device listings, 3 product codes, first listed Oct 5, 2018
- Certification
- Not verified. We have no certification data for this facility yet.
Devices listed as contract work
Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.
| Product code | Device (FDA name) | Class | Category | Role | First listed |
|---|---|---|---|---|---|
| KIP | Formulations, Balanced Salt Solutions | Class I | Hematology | Contract manufacturing | Jun 2, 2020 |
| KIS | Sera, Animal And Human | Class I | Hematology | Contract manufacturing | Oct 5, 2018 |
| KIT | Media And Components, Synthetic Cell And Tissue Culture | Class I | Hematology | Contract manufacturing | Jun 2, 2020 |