Endoch Inc
Country not established
Endoch Inc is a medical device manufacturer, with 355 devices listed in FDA GUDID (FDA Class I and II) as of 14 Nov 2026.
- Devices
- 355
Registry facts
- Registries
- FDA GUDID 355
- Device classes
- FDA Class I 261
- FDA Class II 94
- Identifiers
- DUNS 241382683
What Endoch Inc makes
Endoch Inc manufactures single-use and reusable endoscopic devices, including flexible and rigid biopsy forceps, grasping forceps, scissors, and tissue manipulation tools. Their product line also covers reusable and single-use flexible video colonoscopes and gastroscopes designed for gastrointestinal procedures.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Endoch Inc operates from the United States.
Catalogue
Search and filter all 355 devicesShowing 1-50 of 355
Company details
- DUNS number
- 241382683
Frequently asked questions
How many devices does Endoch Inc have in the registry?
The registry currently lists 355 devices for Endoch Inc. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endoch Inc's devices?
Among its 50 most recently registered devices, Endoch Inc has devices listed in FDA GUDID (50 devices).
What risk classes do Endoch Inc's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Endoch Inc's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endoch Inc in the registry?
The most recently registered devices listed for Endoch Inc include Endoch DBF-2323R, Endoch CS-430T, Endoch EAI-0818 and Endoch DBF-2320AF.