Contract manufacturerVitrolife Inc. (Englewood, CO)ColoradoObstetrics and gynecologyClass II
Vitrolife Inc.
Contract manufacturer ยท Englewood, CO
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3003274090 (openFDA record; or search FDA's registration database)
- FEI number
- 3003274090
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer for export only; Contract manufacturer
- Owner or operator
- VITROLIFE AB (FDA owner/operator no. 9037178)
- Registered address
- 3601 South Inca Street, Englewood, CO 80110
- Contract listings
- 11 device listings, 2 product codes, first listed Nov 12, 2007
- 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 |
|---|---|---|---|---|---|
| MQL | Media, Reproductive | Class II | Obstetrics and gynecology | Contract manufacturing | Nov 12, 2007 |
| QKI | Media, Reproductive, Exempt | Class II | Obstetrics and gynecology | Contract manufacturing | Aug 10, 2020 |