Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012764743

FEI Number

3012764743

Entity Name

CORY LABS

City/State/Country

Alsip, IL, US

Establishment Address

11708 S. Mayfield Ave, Alsip, IL 60803, US

Establishment Type(s)

Manufacture Medical Device,Repack or Relabel Medical Device

Owner / Operator

Cory Labs (Owner Number: 10058360)

Owner / Operator Contact Address

11708 S. Mayfield Ave, Alsip, IL 60803, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Cory Labs

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EFT	Cleanser, Denture, Over The Counter	Dental	Class 1	872.3520	2018-08-31

Official Correspondent

John Khouri

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cory Labs

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K902838	Denture Dynamic'S, Inc.	DENTURE DYNAMIC'S DENTURE MAGIC	1990-09-06

Similar Registrations

Registration Number	Establishment Name	Location
1314819	Haleon US Holdings LLC	East Durham, NY, US
3014545262	LMA SOLUTIONS INC.	Raleigh, NC, US
1058743	REGENT LABS, INC.	Deerfield Bch, FL, US
3009211643	WEIHAI HUIHAI COMMODITY MANUFACTURE CO., LTD.	Weihai Shandong, CN
1821514	KULZER, LLC	SOUTH BEND, IN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012764743. Last updated year: 2026. Please use registration number 3012764743 when referencing this establishment in official correspondence.