MedtechSourcebook

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 codeDevice (FDA name)ClassCategoryRoleFirst listed
FTALight, Surgical, AccessoriesClass IIGeneral and plastic surgeryContract manufacturingOct 8, 2014