Data / Medical devices / Table, Surgical With Orthopedic Accessories, Manual / United States

FDA-registered makers of Table, Surgical With Orthopedic Accessories, Manual in the United States: 20 establishments

Name: FDA-registered makers of Table, Surgical With Orthopedic Accessories, Manual in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

20 establishments in the United States are registered with the FDA to make Table, Surgical With Orthopedic Accessories, Manual (product code JEB). 1 has a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.

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Device: Table, Surgical With Orthopedic Accessories, Manual
Product code: JEB
Country: United States

Makers of Table, Surgical With Orthopedic Accessories, Manual in the United States

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Source
Steris Corporation	Montgomery, AL, United States	Complaint file establishment, Manufacturer	1	March 6, 1991	0	api.fda.gov
A.M. Surgical, Inc.	Nashua, NH, United States	Specification developer	0		0	api.fda.gov
American Benchmark Machine Works	Olympia, WA, United States	Contract manufacturer	0		0	api.fda.gov
Arthro-Positioning Systems LLC	Bogart, GA, United States	Manufacturer	0		0	api.fda.gov
Aspen Surgical Products, Inc.	Caledonia, MI, United States	Complaint file establishment, Specification developer	0		0	api.fda.gov
B & J Medical LLC	Kendallville, IN, United States	Contract manufacturer	0		0	api.fda.gov
Biomet, Inc.	Warsaw, IN, United States	Manufacturer	0		1	api.fda.gov
Depuy Orthopaedics, Inc.	Warsaw, IN, United States	Manufacturer, Specification developer	0		0	api.fda.gov
Depuy Spine, Inc.	Raynham, MA, United States	Specification developer	0		0	api.fda.gov
DePuy Mitek, Inc.	Raynham, MA, United States	Specification developer	0		0	api.fda.gov
Domico Med-Device, LLC	Fenton, MI, United States	Contract manufacturer	0		0	api.fda.gov
General Hospital Supply Corp.	Indian Trail, NC, United States	Specification developer	0		0	api.fda.gov
Globus Medical, Inc.	Audubon, PA, United States	Manufacturer	0		0	api.fda.gov
Innomed, Inc.	Savannah, GA, United States	Specification developer	0		0	api.fda.gov
Match Grade Medical	Neenah, WI, United States	Manufacturer	0		0	api.fda.gov
MEDLINE INDUSTRIES, LP - Northfield	Northfield, IL, United States	Specification developer	0		0	api.fda.gov
Orthopediatrics, Corp	Warsaw, IN, United States	Complaint file establishment, Repackager or relabeler, Specification developer	0		0	api.fda.gov
Stryker Endoscopy	San Jose, CA, United States	Manufacturer	0		0	api.fda.gov
Viant Medical, LLC	Fort Wayne, IN, United States	Contract manufacturer	0		0	api.fda.gov
White Surgical, Inc.	Fort Wayne, IN, United States	Manufacturer, Specification developer	0		0	api.fda.gov

Updated November 3, 2026. 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.