Contract manufacturerLitex Manufacturing, Inc. (Glendale, CA)CaliforniaGeneral and plastic surgeryClass II
Litex Manufacturing, Inc.
Contract manufacturer ยท Glendale, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3010676465 (openFDA record; or search FDA's registration database)
- FEI number
- 3010676465
- Registered for
- FDA registration year 2027
- Establishment types
- Contract manufacturer
- Owner or operator
- Litex Manufacturing, Inc. (FDA owner/operator no. 10045904)
- Registered address
- 820 Thompson Ave Ste 9, Glendale, CA 91201
- Contract listings
- 1 device listings, 1 product codes, first listed Oct 8, 2014
- 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 |
|---|---|---|---|---|---|
| FTA | Light, Surgical, Accessories | Class II | General and plastic surgery | Contract manufacturing | Oct 8, 2014 |