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Authorized Acquisitions LLC: FDA-registered device maker in Mokena, IL, United States, 13 510(k) clearances

Name: Authorized Acquisitions LLC FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Authorized Acquisitions LLC is registered with the FDA (registration 3011277660) in Mokena, IL, United States. It lists 16 device types. The FDA files 13 510(k) clearances under its listings, the newest dated June 10, 2025. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number: 3011277660
Address: 9830 W 190th St Ste J, Mokena, IL, United States, 60448
Owner or operator: Authorized Acquisitions LLC (10052386)
Roles: Repackager or relabeler
First device listed: July 6, 2017
Registered through: 2027

Devices it lists

Device	Product code	Class	Role	Source
Accessories, Arthroscopic	NBH	1	Repackager or relabeler	accessdata.fda.gov
Arthroscope	HRX	2	Repackager or relabeler	accessdata.fda.gov
Bed, Ac-Powered Adjustable Hospital	FNL	2	Repackager or relabeler	accessdata.fda.gov
Blade, Saw, General & Plastic Surgery, Surgical	GFA	1	Repackager or relabeler	accessdata.fda.gov
Camera, Cine, Endoscopic, Without Audio	FWL	1	Repackager or relabeler	accessdata.fda.gov
Electrosurgical, Cutting & Coagulation & Accessories	GEI	2	Repackager or relabeler	accessdata.fda.gov
Endoscope, Accessories, Narrow Band Spectrum	NWB	2	Repackager or relabeler	accessdata.fda.gov
Forceps	HTD	1	Repackager or relabeler	accessdata.fda.gov
Gastroscope And Accessories, Flexible/Rigid	FDS	2	Repackager or relabeler	accessdata.fda.gov
Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment	HWE	1	Repackager or relabeler	accessdata.fda.gov
Insufflator, Laparoscopic	HIF	2	Repackager or relabeler	accessdata.fda.gov
Laparoscope, General & Plastic Surgery	GCJ	2	Repackager or relabeler	accessdata.fda.gov
Light Source, Fiberoptic, Routine	FCW	2	Repackager or relabeler	accessdata.fda.gov
Spreader, Cuff	CBG	1	Repackager or relabeler	accessdata.fda.gov
Table And Attachments, Operating-Room	BWN	1	Repackager or relabeler	accessdata.fda.gov
Tourniquet, Pneumatic	KCY	1	Repackager or relabeler	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
June 10, 2025	K243512	FUJIFILM Endoscope Model EG-840N; FUJIFILM Endoscope Model EG-840T; FUJIFILM Endoscope Model EG-840TP	FDS	Substantially Equivalent	Fujifilm Corporation	accessdata.fda.gov
September 4, 2024	K240142	FUJIFILM Endoscope Model EG-840N; FUJIFILM Endoscope Model EG-840T; FUJIFILM Endoscope Model EG-840TP	FDS	Substantially Equivalent	Fujifilm Corporation	accessdata.fda.gov
January 9, 2013	K123441	STRYKER CROSSFLOW ARTHROSCOPY PUMP	HRX	Substantially Equivalent	Stryker Endoscopy	accessdata.fda.gov
September 5, 2012	K121893	STRYKER SDC3 HD INFORMATION MANAGEMENT SYSTEM	GCJ	Substantially Equivalent	Stryker Endoscopy	accessdata.fda.gov
December 16, 2010	K103536	IBED WIRELESS WITH IBED AWARENESS	FNL	Substantially Equivalent	Stryker Corporation	accessdata.fda.gov
December 19, 2008	K082813	STRYKER LED LIGHTSOURCE	FCW	Substantially Equivalent	Stryker Corp.	accessdata.fda.gov
September 20, 2007	K071859	STRYKER CROSSFIRE SYSTEM	GEI	Substantially Equivalent	Stryker Endoscopy	accessdata.fda.gov
September 22, 2006	K062049	EVIS EXERA II 180 SYSTEM	NWB	Substantially Equivalent	Olympus Medical Systems Corporation	accessdata.fda.gov
September 2, 2005	K050411	ZIMMER A.T.S. 3000 AUTOMATIC TOURNIQUET SYSTEM	KCY	Substantially Equivalent	Zimmer, Inc.	accessdata.fda.gov
February 21, 2001	K003792	STRYKER HEATED INSUFFLATOR TUBE SET	HIF	Substantially Equivalent	Stryker Corp.	accessdata.fda.gov
October 27, 1999	K993045	BARIATRIC LAPAROSCOPE, MODEL 367	GCJ	Substantially Equivalent	Stryker Endoscopy	accessdata.fda.gov
January 11, 1999	K983566	3-CHIP VIDEO CAMERA	GCJ	Substantially Equivalent	Stryker Endoscopy	accessdata.fda.gov
November 28, 1994	K943323	STRYKER SURGICAL INSTRUMENTS AND ACCESSORIES	HRX	Substantially Equivalent	Stryker Corp.	accessdata.fda.gov

Compare with other makers

Updated June 10, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.