Medpro, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Medpro, Inc. makes
Medpro, Inc. manufactures flotation systems and cushions, including the MEDPRO FLOTATION SYSTEM, HEEL/ELBOW FLOTATION CUSHION, FLOTATION UNIT CHAIR, and NEONATAL FLOTATION SYSTEM.
The company's products are Class I devices listed in the FDA 510(k) registry, and Medpro, Inc. is based in the US.
Catalogue
Medpro Flotation System Ref K771824
Regimes: 510(k) Registry: 510(k)Heel/Elbow Flotation Cushion Ref K760870
Regimes: 510(k) Registry: 510(k)Flotation Unit, Chair Ref K760613
Regimes: 510(k) Registry: 510(k)Neonatal Flotation System Ref K772062
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medpro, Inc. have in the registry?
The registry currently lists 4 devices for Medpro, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medpro, Inc.'s devices?
Among its 4 most recently registered devices, Medpro, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Medpro, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Medpro, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Medpro, Inc. in the registry?
The most recently registered devices listed for Medpro, Inc. include MEDPRO FLOTATION SYSTEM, HEEL/ELBOW FLOTATION CUSHION, FLOTATION UNIT, CHAIR and NEONATAL FLOTATION SYSTEM.