Contract manufacturerMARUHO RELUCENT, INC (Santa Rosa, CA)CaliforniaCardiovascularClass III
MARUHO RELUCENT, INC
Contract manufacturer · Santa Rosa, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3012865735 (openFDA record; or search FDA's registration database)
- FEI number
- 3012865735
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Maruho Relucent, Inc (FDA owner/operator no. 10095291)
- Registered address
- 1415 N Dutton Ave Ste C, Santa Rosa, CA 95401
- Contract listings
- 1 device listings, 1 product codes, first listed Feb 19, 2026
- 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 |
|---|---|---|---|---|---|
| NIM | Stent, Carotid | Class III | Cardiovascular | Contract manufacturing | Feb 19, 2026 |