Medsentry Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Medsentry Corp. makes
Medsentry Corp. makes flotation and soft-touch systems, specifically the Medsentry Flotation System and the Medsentry SoftTouch System.
These devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Medsentry Flotation System Ref K863152
Regimes: 510(k) Registry: 510(k)Medsentry Softouch System Ref K844499
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medsentry Corp. have in the registry?
The registry currently lists 2 devices for Medsentry Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medsentry Corp.'s devices?
Among its 2 most recently registered devices, Medsentry Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Medsentry Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medsentry Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medsentry Corp. in the registry?
The most recently registered devices listed for Medsentry Corp. include MEDSENTRY FLOTATION SYSTEM and MEDSENTRY SOFTOUCH SYSTEM.