Contract manufacturerOncore Manufacturing, LLC dba NEOTech (Fremont, CA)CaliforniaGeneral and plastic surgeryOphthalmicClass II
Oncore Manufacturing, LLC dba NEOTech
Contract manufacturer · Fremont, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3009462521 (openFDA record; or search FDA's registration database)
- FEI number
- 3009462521
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Oncore Manufacturing, LLC (FDA owner/operator no. 10042195)
- Registered address
- 48119 Warm Springs Blvd, Fremont, CA 94539
- Contract listings
- 1 device listings, 2 product codes, first listed Feb 12, 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 |
|---|---|---|---|---|---|
| GEX | Powered Laser Surgical Instrument | Class II | General and plastic surgery | Contract manufacturing | Feb 12, 2026 |
| HQF | Laser, Ophthalmic | Class II | Ophthalmic | Contract manufacturing | Feb 12, 2026 |