Simondr, Inc.
Country not established
- Devices
- 1
What Simondr, Inc. makes
Simondr, Inc. manufactures the SIMONDR DRP, which is a Class II medical device.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Simondr Drp Ref K093790
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Simondr, Inc. have in the registry?
The registry currently lists 1 device for Simondr, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Simondr, Inc.'s devices?
Among its 1 most recently registered device, Simondr, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Simondr, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Simondr, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Simondr, Inc. in the registry?
The most recently registered devices listed for Simondr, Inc. include SIMONDR DRP.