Data / Medical devices / Component, External, Limb, Ankle/Foot / United States

FDA-registered makers of Component, External, Limb, Ankle/Foot in the United States: 27 establishments

Name: FDA-registered makers of Component, External, Limb, Ankle/Foot in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

27 establishments in the United States are registered with the FDA to make Component, External, Limb, Ankle/Foot (product code ISH). 0 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.

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Device: Component, External, Limb, Ankle/Foot
Product code: ISH
Country: United States

Makers of Component, External, Limb, Ankle/Foot in the United States

Maker	Location	Role	Recall events	Source
Alps South LLC	Saint Petersburg, FL, United States	Manufacturer	0	api.fda.gov
BioSkin LLC	Ashland, OR, United States	Manufacturer, Repackager or relabeler	0	api.fda.gov
Blatchford, Inc.	Miamisburg, OH, United States	Manufacturer	0	api.fda.gov
Brownmed	Spirit Lake, IA, United States	Manufacturer	0	api.fda.gov
COYOTE O&P, Inc	Boise, ID, United States	Manufacturer	0	api.fda.gov
College Park Industries	Warren, MI, United States	Manufacturer	1	api.fda.gov
Deroyal Industries, Inc.	Powell, TN, United States	Complaint file establishment, Specification developer	0	api.fda.gov
Fillauer, LLC	Chattanooga, TN, United States	Manufacturer	0	api.fda.gov
Fillauer Composites	Salt Lake City, UT, United States	Manufacturer	0	api.fda.gov
Human Motion Technologies LLC	Pittsburgh, PA, United States	Manufacturer, Specification developer	0	api.fda.gov
Ifit Prosthetics LLC	Oconomowoc, WI, United States	Manufacturer	0	api.fda.gov
Impulse Technology LLC	State College, PA, United States	Manufacturer, Specification developer	0	api.fda.gov
Kinetic Research	Tampa, FL, United States	Manufacturer	0	api.fda.gov
Limber Prosthetics, Inc.	San Diego, CA, United States	Complaint file establishment, Manufacturer	0	api.fda.gov
Motion Control, Inc.	Salt Lake City, UT, United States	Manufacturer	0	api.fda.gov
O&M Halyard, Inc.	Alpharetta, GA, United States	Complaint file establishment, Manufacturer, Specification developer	0	api.fda.gov
Ossur Americas	West Deptford, NJ, United States	Contract manufacturer, Repackager or relabeler	0	api.fda.gov
Otto Bock Healthcare LP	Salt Lake City, UT, United States	Manufacturer, Specification developer	0	api.fda.gov
Ossur Orlando	Orlando, FL, United States	Contract manufacturer	0	api.fda.gov
Professional Products, Inc.	Defuniak Spgs, FL, United States	Manufacturer, Repackager or relabeler	0	api.fda.gov
Proteor Usa	Tempe, AZ, United States	Complaint file establishment, Manufacturer	0	api.fda.gov
PROTEOR USA, Gunnison	Gunnison, UT, United States	Manufacturer	1	api.fda.gov
Restorative Care Of America, Inc.	Saint Petersburg, FL, United States	Manufacturer	0	api.fda.gov
ST&G Usa Corporation / Choi	Brea, CA, United States	Repackager or relabeler, Specification developer	0	api.fda.gov
Trulife, Inc.	Bellingham, WA, United States	Manufacturer	0	api.fda.gov
WW-West	Mesa, AZ, United States	Manufacturer	0	api.fda.gov
WillowWood Global LLC	Mt Sterling, OH, United States	Manufacturer	0	api.fda.gov

Updated November 2, 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.