Sentron Medical, Inc.
Country not established
- Devices
- 1
What Sentron Medical, Inc. makes
Sentron Medical, Inc. manufactures the SIS Hernia Repair Device, a surgical implant designed for hernia repair procedures.
The SIS Hernia Repair Device 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
Sis Hernia Repair Device Ref K974540
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sentron Medical, Inc. have in the registry?
The registry currently lists 1 device for Sentron Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sentron Medical, Inc.'s devices?
Among its 1 most recently registered device, Sentron Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sentron Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sentron Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sentron Medical, Inc. in the registry?
The most recently registered devices listed for Sentron Medical, Inc. include SIS HERNIA REPAIR DEVICE.