Contract manufacturerDUPACO, INC. (Oceanside, CA)CaliforniaAnesthesiologyRadiologyClass IClass II
DUPACO, INC.
Contract manufacturer · Oceanside, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 2021969 (openFDA record; or search FDA's registration database)
- FEI number
- 2021969
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer; Repackager or relabeler
- Owner or operator
- DUPACO, INC. (FDA owner/operator no. 2021969)
- Registered address
- 4144 AVENIDA DE LA PLATA, Oceanside, CA 92056
- Contract listings
- 3 device listings, 2 product codes, first listed Mar 2, 2000
- 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 |
|---|---|---|---|---|---|
| CCX | Support, Patient Position | Class I | Anesthesiology | Contract manufacturing | Mar 2, 2000 |
| JAQ | System, Applicator, Radionuclide, Remote-Controlled | Class II | Radiology | Contract manufacturing | Nov 30, 2012 |