United States Endoscopy
Country not established
- Devices
- 1
What United States Endoscopy makes
United States Endoscopy manufactures monofilament polypectomy snares, which are single‑strand loop devices used during endoscopic procedures to resect gastrointestinal polyps.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Monofilament Polypectomy Snare Ref K140763
510(k) 510(k)
Frequently asked questions
How many devices does United States Endoscopy have in the registry?
The registry currently lists 1 device for United States Endoscopy. Devices recorded under merged duplicate company entries are counted once.
Which registries list United States Endoscopy's devices?
Among its 1 most recently registered device, United States Endoscopy has devices listed in FDA 510(k) (1 device).
What risk classes do United States Endoscopy's devices fall under?
Among its 1 most recently registered device, the classes recorded for United States Endoscopy's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from United States Endoscopy in the registry?
The most recently registered devices listed for United States Endoscopy include MONOFILAMENT POLYPECTOMY SNARE.