Rokonics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Rokonics, Inc. makes
Rokonics, Inc. manufactures the ROKONICS SENTRY MODEL 8500 and ROKONICS 8500 devices.
These Class II devices are listed in the FDA 510(k) registry, and the company is based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Rokonics Sentry Model 8500 Ref K851819
Regimes: 510(k) Registry: 510(k)Rokonics 8500 Ref K871576
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rokonics, Inc. have in the registry?
The registry currently lists 2 devices for Rokonics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rokonics, Inc.'s devices?
Among its 2 most recently registered devices, Rokonics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Rokonics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Rokonics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rokonics, Inc. in the registry?
The most recently registered devices listed for Rokonics, Inc. include ROKONICS SENTRY MODEL 8500 and ROKONICS 8500.