Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2028483

FEI Number

1000125174

Entity Name

KLM LABORATORIES, INC.

City/State/Country

Valencia, CA, US

Establishment Address

28280 Alta Vista Ave, Valencia, CA 91355, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

klm laboratories, inc. (Owner Number: 9005017)

Owner / Operator Contact Address

28280 ALTA VISTA AVENUE, --, Valencia, CA 91355, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Richie Brace KLM Functional AFO

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KYS	Insoles, Medical	General Hospital	Class 1	880.6280	1992-06-10

Official Correspondent

scott marshall

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

klm laboratories, inc.

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3015436904	CPO Labs, LLC	Peoria, IL, US
2519342	Hapad, Inc	Bethel Park, PA, US
3004992834	AMFIT, LLC.	Vancouver, WA, US
3010508273	LIANG CHENG SPORTING GOODS COMPANY LIMITED	Ben Cat Town Binh Duong, VN
3014943293	PREFERRED INDUSTRIES, INC.	Fort Lauderdale, FL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2028483. Last updated year: 2026. Please use registration number 2028483 when referencing this establishment in official correspondence.