Contract manufacturerCARL ZEISS MEDITEC INC (Dublin, CA)CaliforniaOphthalmicClass II
CARL ZEISS MEDITEC INC
Contract manufacturer ยท Dublin, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 2918630 (openFDA record; or search FDA's registration database)
- FEI number
- 2918630
- Registered for
- FDA registration year 2026
- Establishment types
- Specification developer; Manufacturer; Contract manufacturer; Repackager or relabeler
- Owner or operator
- Carl Zeiss Meditec AG (Jena) (FDA owner/operator no. 9053564)
- Registered address
- 5300 Central Parkway, Dublin, CA 94568
- Contract listings
- 2 device listings, 2 product codes, first listed Oct 19, 2012
- 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 |
|---|---|---|---|---|---|
| HKI | Camera, Ophthalmic, Ac-Powered | Class II | Ophthalmic | Contract manufacturing | Oct 19, 2012 |
| OBO | Tomography, Optical Coherence | Class II | Ophthalmic | Contract manufacturing | Oct 19, 2012 |