Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015436904

FEI Number

3015436904

Entity Name

CPO Labs, LLC

City/State/Country

Peoria, IL, US

Establishment Address

725 W Main St, Peoria, IL 61606, US

Establishment Type(s)

Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

CPO Labs LLC (Owner Number: 10060090)

Owner / Operator Contact Address

741 W Main St, Peoria, IL 61606, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KYS	Insoles, Medical	General Hospital	Class 1	880.6280	2019-03-28

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CPO Labs LLC

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 3015436904. Last updated year: 2026. Please use registration number 3015436904 when referencing this establishment in official correspondence.