Contract manufacturerCODAN US CORP. (Santa Ana, CA)CaliforniaGeneral hospitalGastroenterology and urologyClass II
CODAN US CORP.
Contract manufacturer · Santa Ana, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 2016945 (openFDA record; or search FDA's registration database)
- FEI number
- 2016945
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer; Remanufacturer
- Owner or operator
- CODAN US Corporation (FDA owner/operator no. 8010060)
- Registered address
- 3501 WEST SUNFLOWER AVE., Santa Ana, CA 92704
- Contract listings
- 8 device listings, 4 product codes, first listed Nov 29, 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 |
|---|---|---|---|---|---|
| FPA | Set, Administration, Intravascular | Class II | General hospital | Contract manufacturing | Nov 29, 2007 |
| GCX | Apparatus, Suction, Operating-Room, Wall Vacuum Powered | Class II | General hospital | Contract manufacturing | Jul 28, 2010 |
| KNT | Tubes, Gastrointestinal (And Accessories) | Class II | Gastroenterology and urology | Contract manufacturing | Jul 27, 2010 |
| LHI | Set, I.V. Fluid Transfer | Class II | General hospital | Contract manufacturing | Nov 29, 2007 |