FDA Registration
Active
🇺🇸 United States
Nutek Bravo, Hayward
Reg #: 3015542130
·
FEI: 3015542130
·
Expires 2026
Products
5
Proprietary Names
1
Establishment Types
1
Classifications
5
Registration Details
- Registration Name
- Nutek Bravo, Hayward
- Registration Number
- 3015542130
- FEI Number
- 3015542130
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- No
- Address
- 26545 Corporate Ave
- City
- Hayward
- State
- CA
- ZIP
- 94545
- Country
- US
Owner / Operator
- Firm Name
- Nutek Bravo
- Operator Number
- 10081366
- Address
- 26545 Corporate Ave
- City
- Hayward
- State
- CA
- Postal Code
- 94545
- Country
- US
- Correspondent
- Thomas Green
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Device, Irrigation, Ocular Surgery | KYG | Class 1 | Ophthalmic | No | 2024-08-01 |
| Device, Hemostasis, Vascular | MGB | Class 3 | Unknown | No | 2023-10-27 |
| Filler, Bone Void, Calcium Compound | MQV | Class 2 | Orthopedic | No | 2025-06-06 |
| Cannula, Injection | FGY | Class 1 | General, Plastic Surgery | No | 2024-02-02 |
| Wound Dressing With Animal-Derived Material(S) | KGN | Class U | Unknown | No | 2025-04-22 |
Proprietary Names
ClearVu 2.7 Blunt; ClearVu 2.7 Sharp; DryVu; Exstravastopper; TwoVu ST-5; TwoVu ST-6; TwoVu ST-6-130; TwoVu ST-6-134; Tw
Establishment Types
Sterilize Medical Device for Another Party (Contract Sterilizer)