Contract manufacturerRH USA, INC. (Livermore, CA)CaliforniaGeneral and plastic surgeryPhysical medicineOphthalmicClass IIClass I
RH USA, INC.
Contract manufacturer · Livermore, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 2953684 (openFDA record; or search FDA's registration database)
- FEI number
- 3001611958
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- RH USA, INC. (FDA owner/operator no. 9061116)
- Registered address
- 455 N Canyons Pkwy Suite B, Livermore, CA 94551
- Contract listings
- 7 device listings, 5 product codes, first listed Jun 25, 2018
- 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 |
|---|---|---|---|---|---|
| GEX | Powered Laser Surgical Instrument | Class II | General and plastic surgery | Contract manufacturing | Jun 25, 2018 |
| ISA | Massager, Therapeutic, Electric | Class I | Physical medicine | Contract manufacturing | May 8, 2025 |
| ONG | Powered Laser Surgical Instrument With MicrobeamFractional Output | Class II | General and plastic surgery | Contract manufacturing | Mar 31, 2025 |
| PAY | Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction | Class II | General and plastic surgery | Contract manufacturing | May 8, 2025 |
| QIU | Intense Pulsed Light Device For Managing Dry Eye | Class II | Ophthalmic | Contract manufacturing | Mar 31, 2025 |