Contract manufacturerVitrolife Inc. (San Diego, CA)CaliforniaObstetrics and gynecologyClass II
Vitrolife Inc.
Contract manufacturer ยท San Diego, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 2031824 (openFDA record; or search FDA's registration database)
- FEI number
- 3002757762
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer
- Owner or operator
- VITROLIFE AB (FDA owner/operator no. 9037178)
- Registered address
- 4940 Carroll Canyon Rd Ste 100, San Diego, CA 92121
- Contract listings
- 1 device listings, 1 product codes, first listed Dec 5, 2022
- 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 |
|---|---|---|---|---|---|
| PUC | Microtools, Assisted Reproduction (Pipettes), Exempt | Class II | Obstetrics and gynecology | Contract manufacturing | Dec 5, 2022 |