Data / Medical devices / Accessories, Photographic, For Endoscope (Exclude Light Sources) / United States

FDA-registered makers of Accessories, Photographic, For Endoscope (Exclude Light Sources) in the United States: 20 establishments

Name: FDA-registered makers of Accessories, Photographic, For Endoscope (Exclude Light Sources) 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 Accessories, Photographic, For Endoscope (Exclude Light Sources) (product code FEM). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device: Accessories, Photographic, For Endoscope (Exclude Light Sources)
Product code: FEM
Country: United States

Makers of Accessories, Photographic, For Endoscope (Exclude Light Sources) in the United States

Maker	Location	Role	Source
Arthrex, Inc.	Naples, FL, United States	Specification developer	api.fda.gov
Aspen Surgical Products, Inc.	Caledonia, MI, United States	Complaint file establishment, Specification developer	api.fda.gov
Arthrex, Inc.	Ave Maria, FL, United States	Contract manufacturer, Contract sterilizer	api.fda.gov
Boston Scientific Corporation	Marlborough, MA, United States	Specification developer	api.fda.gov
Boston Scientific Corporation	Saint Paul, MN, United States	Complaint file establishment, Manufacturer	api.fda.gov
Clarus Medical, LLC.	Minneapolis, MN, United States	Manufacturer, Repackager or relabeler	api.fda.gov
DePuy Mitek, Inc.	Raynham, MA, United States	Specification developer	api.fda.gov
Endocraft LLC.	Newton, MA, United States	Manufacturer	api.fda.gov
Geotec, Inc.	Warwick, RI, United States	Contract manufacturer	api.fda.gov
Highridge Medical, LLC	Westminster, CO, United States	Specification developer	api.fda.gov
Innomed, Inc.	Savannah, GA, United States	Specification developer	api.fda.gov
Karl Storz Imaging, Inc.	Goleta, CA, United States	Contract manufacturer	api.fda.gov
Linvatec Corporation	Largo, FL, United States	Specification developer	api.fda.gov
National Advanced Endoscopy Devices, Inc.	Canoga Park, CA, United States	Manufacturer	api.fda.gov
Olive Branch Distribution Center	Olive Branch, MS, United States	Contract manufacturer	api.fda.gov
Precision Optics Corp.	Gardner, MA, United States	Contract manufacturer	api.fda.gov
Richard Wolf Medical Instruments Corp.	Vernon Hills, IL, United States	Contract manufacturer	api.fda.gov
Santa Barbara Imaging Systems	Goleta, CA, United States	Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer	api.fda.gov
Stryker Endoscopy	San Jose, CA, United States	Manufacturer	api.fda.gov
Transamerican Technologies International	San Ramon, CA, United States	Manufacturer	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.