Litex Manufacturing, Inc.

FDA Device Registration & Listing · Glendale, CA, US · Registration 3010676465

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3010676465
FEI Number
3010676465
Entity Name
Litex Manufacturing, Inc.
City/State/Country
Glendale, CA, US
Establishment Address
820 Thompson Ave Ste 9, Glendale, CA 91201, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Litex Manufacturing, Inc. (Owner Number: 10045904)
Owner / Operator Contact Address
1501 Sunshine Drive, Glendale, CA 91208, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K142386
PMA Number
N/A

All Registered Proprietary Names

Devon Operating Room Universal Light Adaptor Operating Room Universal Light Handle Operating Room Universal Light Camera Adator

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MDM Instrument, Manual, Surgical, General Use General, Plastic Surgery Class 1 878.4800 2014-01-10
FTA Light, Surgical, Accessories General, Plastic Surgery Class 2 878.4580 2014-10-08

Official Correspondent

Noel Gharibian

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Litex Manufacturing, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010676465. Last updated year: 2026. Please use registration number 3010676465 when referencing this establishment in official correspondence.
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