Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013710866

FEI Number

3013710866

Entity Name

TOTEX MANUFACTURING INC

City/State/Country

Torrance, CA, US

Establishment Address

3050 Lomita Blvd, Torrance, CA 90505, US, FDA room, Torrance, CA 90505, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Totex Manufacturing Inc (Owner Number: 10061778)

Owner / Operator Contact Address

3050 Lomita Blvd, Torrance, CA 90505, US, FDA room, Torrance, CA 90505, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Zimmer Biomet

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MOQ	Battery, Replacement, Rechargeable	General, Plastic Surgery	Class 1	878.4820	2019-11-19

Official Correspondent

Victor Shih

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Totex Manufacturing Inc

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013710866. Last updated year: 2026. Please use registration number 3013710866 when referencing this establishment in official correspondence.