Skip to content

US Endoscopy

Country not established

US Endoscopy is a medical device manufacturer, with 1,023 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II and I) as of 13 Nov 2026.

Devices
1,023

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 1,022
  • EUDAMED 95
  • FDA 510(k) 1

A device listed in two registries counts in both.

Device classes
  • FDA Class II 970
  • FDA Class I 53
Identifiers
  • DUNS 627879687

What US Endoscopy makes

US Endoscopy manufactures single-use and reusable devices for gastrointestinal and airway procedures, including endoscopic retrieval baskets for foreign body removal, dilation balloons for biliary/gastrointestinal applications, and endoscopic clips for long-term tissue approximation. Their portfolio also includes endoscope working-channel valves, electrosurgical handpieces, cleaning utensils, and channel support kits designed to enhance procedural efficiency and safety. Examples include retrieval baskets like the Roth Net Platinum, dilation balloons such as the Small Wonder, and endoscopic clips like the Padlock Clip Pro-Select.

The company’s devices are classified under FDA regulations as either Class I or Class II, with all products listed in the FDA’s Unique Device Identification (UDI) database. These products are intended for use in the United States, adhering to applicable medical device standards and requirements for their respective classifications.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1,023

Newest first, rows 1-50 of 1,023

Search and filter all 1,023 devices
Skip device list

Rows 1-50 of 1,023

Showing 1-50 of 1,023

Company details

DUNS number
627879687
Phone
+1(800)548-4873

Frequently asked questions

How many devices does US Endoscopy have in the registry?

The registry currently lists 1023 devices for US Endoscopy. Devices recorded under merged duplicate company entries are counted once.

Which registries list US Endoscopy's devices?

Among its 50 most recently registered devices, US Endoscopy has devices listed in EUDAMED (6 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do US Endoscopy's devices fall under?

Among its 50 most recently registered devices, the classes recorded for US Endoscopy's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from US Endoscopy in the registry?

The most recently registered devices listed for US Endoscopy include Duoswift 00711600, SmartBand EMR Kit SBEMRK94, SmartBand EMR Pack SBEMRP94 and SmartBand SafeGrip Multi-Band Ligation Kit SLK6LF.

Generated automatically from registry data and not verified by a human reviewer.