Rendoscopy, Inc.
Country not established
- Devices
- 1
What Rendoscopy, Inc. makes
Rendoscopy, Inc. manufactures the GENTLE COLON (Revision 2.0), a device designed for colonoscopy procedures, intended to improve patient comfort and procedural efficiency during examination.
The GENTLE COLON (Revision 2.0) is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Gentle Colon (Revision 2.0) Ref K061532
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rendoscopy, Inc. have in the registry?
The registry currently lists 1 device for Rendoscopy, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rendoscopy, Inc.'s devices?
Among its 1 most recently registered device, Rendoscopy, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Rendoscopy, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Rendoscopy, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rendoscopy, Inc. in the registry?
The most recently registered devices listed for Rendoscopy, Inc. include GENTLE COLON (REVISION 2.0).