Mentor Urology, Inc.
Country not established
- Devices
- 1
What Mentor Urology, Inc. makes
Mentor Urology, Inc. manufactures the Triple Rib Occlusion Wrap, a device designed to treat male incontinence by providing external urethral compression. This product is intended for use in patients requiring mechanical support to control urine leakage.
The Triple Rib Occlusion Wrap is classified as a Class I medical device under FDA regulations and is authorised through the 510(k) clearance process. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mentor Urology, Inc. have in the registry?
The registry currently lists 1 device for Mentor Urology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mentor Urology, Inc.'s devices?
Among its 1 most recently registered device, Mentor Urology, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mentor Urology, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mentor Urology, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mentor Urology, Inc. in the registry?
The most recently registered devices listed for Mentor Urology, Inc. include MENTOR UROLOGY TRIPLE RIB OCCLUSION WRAP FOR MALE INCONTINENCE.