FDA Registration
Active
🇺🇸 United States
DUPACO, INC.
Reg #: 2021969
·
FEI: 2021969
·
Expires 2026
Products
5
Proprietary Names
9
Establishment Types
3
Classifications
5
Registration Details
- Registration Name
- DUPACO, INC.
- Registration Number
- 2021969
- FEI Number
- 2021969
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- No
- Address
- 4144 AVENIDA DE LA PLATA
- City
- OCEANSIDE
- State
- CA
- ZIP
- 92056
- Country
- US
Owner / Operator
- Firm Name
- DUPACO, INC.
- Operator Number
- 2021969
- Address
- 4144 AVENIDA DE LA PLATA, --
- City
- OCEANSIDE
- State
- CA
- Postal Code
- 92056
- Country
- US
- Correspondent
- GREGORY - JORDAN
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| System, Applicator, Radionuclide, Remote-Controlled | JAQ | Class 2 | Radiology | No | 2012-11-30 |
| Support, Patient Position | CCX | Class 1 | Anesthesiology | No | 2000-03-02 |
| Fiber, Medical, Absorbent | FRL | Class 1 | General Hospital | No | 2022-12-07 |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | Class 1 | Ophthalmic | No | 2001-06-14 |
| Shield, Eye, Radiological | IWS | Class 1 | Radiology | No | 2005-06-24 |
Proprietary Names
SAVI Spacer
SAVI Prep Device
ProneConnect Head Positioning System
PRONE VIEW PROTECTIVE HELMET SYSTEM
ProneCam Head Cushion
SAVI Applicator Kit
HK SUPER ABSORBANT PADS
OPTI-GARD EYE PROTECTOR
LASER OPTI-GARD
Establishment Types
Manufacture Medical Device for Another Party (Contract Manufacturer)
Manufacture Medical Device
Repack or Relabel Medical Device