Data / Medical devices / Chair And Table, Medical / United States

FDA-registered makers of Chair And Table, Medical in the United States: 24 establishments

Name: FDA-registered makers of Chair And Table, Medical in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

24 establishments in the United States are registered with the FDA to make Chair And Table, Medical (product code KMN). 0 have 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: Chair And Table, Medical
Product code: KMN
Country: United States

Makers of Chair And Table, Medical in the United States

Maker	Location	Role	Recall events	Source
Advanced Instrumentations, Inc.	Miami, FL, United States	Manufacturer	0	api.fda.gov
ASP Global, LLC	Austell, GA, United States	Specification developer	0	api.fda.gov
AmFab Co., LLC	Richland, MI, United States	Manufacturer	0	api.fda.gov
Bird & Cronin, LLC	Eagan, MN, United States	Manufacturer	0	api.fda.gov
Champion MFG, INC.	Ocala, FL, United States	Manufacturer	0	api.fda.gov
Clinton Industries, Inc	York, PA, United States	Manufacturer, Remanufacturer	0	api.fda.gov
Djo, LLC	Carlsbad, CA, United States	Specification developer	0	api.fda.gov
Fabrication Ent., Inc.	Elmsford, NY, United States	Manufacturer	0	api.fda.gov
Hausmann Enterprises, LLC	Northvale, NJ, United States	Manufacturer, Repackager or relabeler	0	api.fda.gov
ICARE MEDICAL GROUP USA, Inc	Gothenburg, NE, United States	Manufacturer	0	api.fda.gov
Intensa, Inc.	High Point, NC, United States	Manufacturer	0	api.fda.gov
JEDMED Instrument Company	Saint Louis, MO, United States	Manufacturer, Repackager or relabeler	0	api.fda.gov
Knu, LLC	Leland, MS, United States	Manufacturer	0	api.fda.gov
Knu, LLC	Cannelton, IN, United States	Manufacturer	0	api.fda.gov
Lloyd Table Co.	Lisbon, IA, United States	Manufacturer, Repackager or relabeler	0	api.fda.gov
MEDLINE INDUSTRIES, LP - Northfield	Northfield, IL, United States	Specification developer	0	api.fda.gov
MP Seating Inc.	Elkhart, IN, United States	Manufacturer	0	api.fda.gov
Nova Ortho-Med, Inc.	North Aurora, IL, United States	Specification developer	0	api.fda.gov
Oakworks, Inc.	New Freedom, PA, United States	Manufacturer	0	api.fda.gov
Pivotal Health Solutions	Watertown, SD, United States	Manufacturer	0	api.fda.gov
Pivotal Health Solutions	Springfield, OR, United States	Manufacturer	0	api.fda.gov
REACT Innovations	Charlotte, NC, United States	Manufacturer	0	api.fda.gov
Stryker Medical	Portage, MI, United States	Complaint file establishment, Specification developer	1	api.fda.gov
Wieland Designs Inc.	Goshen, IN, United States	Contract manufacturer	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.