Douglas Bueschel
Country not established
- Devices
- 1
What Douglas Bueschel makes
Douglas Bueschel manufactures the Kugel Hernia Patch, a surgical mesh device used for hernia repair, designed to reinforce weakened abdominal wall tissue and promote tissue integration.
The Kugel Hernia Patch is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Kugel Hernia Patch Ref K963141
510(k) 510(k)
Frequently asked questions
How many devices does Douglas Bueschel have in the registry?
The registry currently lists 1 device for Douglas Bueschel. Devices recorded under merged duplicate company entries are counted once.
Which registries list Douglas Bueschel's devices?
Among its 1 most recently registered device, Douglas Bueschel has devices listed in FDA 510(k) (1 device).
What risk classes do Douglas Bueschel's devices fall under?
Among its 1 most recently registered device, the classes recorded for Douglas Bueschel's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Douglas Bueschel in the registry?
The most recently registered devices listed for Douglas Bueschel include KUGEL HERNIA PATCH.