Mediscitec, Inc.
United StatesFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pentaborn Ref K072447
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mediscitec, Inc. have in the registry?
The registry currently lists 1 device for Mediscitec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mediscitec, Inc.'s devices?
Among its 1 most recently registered device, Mediscitec, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mediscitec, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mediscitec, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mediscitec, Inc. in the registry?
The most recently registered devices listed for Mediscitec, Inc. include PENTABORN.