Data / Medical devices / Camera, Cine, Endoscopic, Without Audio

Camera, Cine, Endoscopic, Without Audio (FWL): 19 FDA-registered makers in 4 countries

Name: FDA-registered makers of Camera, Cine, Endoscopic, Without Audio
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

19 establishments in 4 countries are registered with the FDA to make Camera, Cine, Endoscopic, Without Audio (product code FWL, Class 1, 21 CFR 878.4160). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on June 14, 1995, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code: FWL
Device class: 1
Regulation: 878.4160
Medical specialty: General, Plastic Surgery

Makers by country

Country	Makers
United States	9
China	6
Germany	3
South Korea	1

Makers of Camera, Cine, Endoscopic, Without Audio

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

Maker	Location	Role	Source
Anhui Shiyin Photoelectric Instrument Co., Ltd.	Suzhou Anhui, China	Manufacturer	api.fda.gov
Arthrex Logistic Center	Fort Myers, FL, United States	Manufacturer	api.fda.gov
Beijing Fanxing Guangdian Medical Treatment Equipment Co Ltd	Beijing, China	Contract manufacturer, Manufacturer	api.fda.gov
Firefly Global	Belmont, MA, United States	Manufacturer	api.fda.gov
Hebumedical GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Henke-Sass Wolf, GMBH.	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	api.fda.gov
Hosmed Inc.	Doral, FL, United States	Manufacturer, Repackager or relabeler	api.fda.gov
Hoogland Spine Products GmbH	Unterfoehring Munich Bavaria, Germany	Specification developer	api.fda.gov
Inthesmart Co., Ltd.	JONGRO-GU Seoul, South Korea	Manufacturer	api.fda.gov
Novaprobe Inc.	Lansdale, PA, United States	Manufacturer	api.fda.gov
Perioview, LLC	Surprise, AZ, United States	Manufacturer	api.fda.gov
Pure Novamed Inc	Long Beach, CA, United States	Manufacturer, Repackager or relabeler	api.fda.gov
Shenzhen Tuyou Medical Imaging Co., Ltd.	Shenzhen Guangdong, China	Contract manufacturer, Manufacturer	api.fda.gov
Stryker Corp.	Kalamazoo, MI, United States	Contract manufacturer	api.fda.gov
Stryker Manufacturing Kalamazoo	Portage, MI, United States	Contract manufacturer	api.fda.gov
Taevas Life Sciences Inc	Princeton, NJ, United States	Manufacturer	api.fda.gov
Tonglu Youshi Medical Instrument Co.,Ltd	Tonglu Zhejiang, China	Manufacturer	api.fda.gov
Xuzhou Hengjia Electronic Technology Co., Ltd.	Xuzhou Jiangsu, China	Manufacturer	api.fda.gov
Xuzhou AKX Electronic Science and Technology Co., Ltd	Xuzhou City Jiangsu, China	Manufacturer	api.fda.gov

Updated June 14, 1995. 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.