Togard, Inc.
Country not established
- Devices
- 1
What Togard, Inc. makes
Togard, Inc. manufactures the TOGUARD device, a Class I medical product designed for specific clinical applications in wound care or infection prevention.
The TOGUARD device is regulated under the FDA’s 510(k) pathway as a Class I product and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Toguard Ref K790652
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Togard, Inc. have in the registry?
The registry currently lists 1 device for Togard, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Togard, Inc.'s devices?
Among its 1 most recently registered device, Togard, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Togard, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Togard, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Togard, Inc. in the registry?
The most recently registered devices listed for Togard, Inc. include TOGUARD.