Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1831301

FEI Number

1831301

Entity Name

APPLIED LABORATORIES, INC.

City/State/Country

COLUMBUS, IN, US

Establishment Address

3240 N. Indianapolis Rd., COLUMBUS, IN 47201, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Applied Laboratories, Inc. (Owner Number: 1831301)

Owner / Operator Contact Address

3240 NORTH INDIANAPOLIS RD., P.O. BOX 2127, Columbus, IN 47201, 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
OUJ	High Level Disinfection Reprocessing Instrument For Ultrasonic Transducers, Mist	Radiology	Class 2	892.1570	2011-10-17
LFD	Saliva, Artificial	Unknown	Class U	N/A	2025-12-05
FRO	Dressing, Wound, Drug	Unknown	Class U	N/A	2010-12-06
FRO	Dressing, Wound, Drug	Unknown	Class U	N/A	2019-11-06
NUC	Lubricant, Personal	Obstetrics/Gynecology	Class 2	884.5300	2018-08-07
KCJ	Applicator, Ent	Ear, Nose, Throat	Class 1	874.5220	2019-07-22
NUC	Lubricant, Personal	Obstetrics/Gynecology	Class 2	884.5300	2013-12-02
PUN	Lice Removal Kit Containing A Solution	General Hospital	Class 1	880.5960	2023-09-29

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Applied Laboratories, Inc.

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
K150256	Argentum Medical	SILVERLON BURN CONTACT DRESSINGS	2015-04-30
K050212	Qualis, Inc.	PERSONAL WARMING JELLY	2005-03-17

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0003-06	B. Braun Medical, Inc.	U	D-Stat Dry Hemostatic Bandage. The product is an adhesive bandage.
Z-0038-2025	3M Company Health Care Business 3m Center	U	3M Tegaderm CHG, Chlorhexidine Gluconate I.V. Securement Dressing, REF 1658R

Similar Registrations

Registration Number	Establishment Name	Location
3008894376	NANOSONICS, INC.	Indianapolis, IN, US
3006564498	NANOSONICS LIMITED	Macquarie Park New South Wales, AU
3014469173	CONTINENTAL MANUFACTURING CHEMIST	Huxley, IA, US
3007617180	CANADIAN DRY STORAGE LTD.	Richmond British Columbia, CA
3030049002	ROWPAR PHARMACEUTICALS INC.	Bridgewater, NJ, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1831301. Last updated year: 2026. Please use registration number 1831301 when referencing this establishment in official correspondence.