Uhi Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Uhi Corp. makes
Uhi Corp. manufactures air fluidized support systems, including the Clinitron Air Fluidized Support J-101UD and Clinitron Air Fluidized Support System, designed for patient positioning and pressure redistribution. They also produce barrier burn sheets for wound care applications.
The company’s products are regulated under FDA Class I and Class II classifications, with some devices authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Clinitron Air Fluidized Support J-101UD Ref K843389
Regimes: 510(k) Registry: 510(k)Clinitron Air Fluidized Support System Ref K813584
Regimes: 510(k) Registry: 510(k)Barrier Burn Sheet Ref K821835
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Uhi Corp. have in the registry?
The registry currently lists 3 devices for Uhi Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Uhi Corp.'s devices?
Among its 3 most recently registered devices, Uhi Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Uhi Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Uhi Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Uhi Corp. in the registry?
The most recently registered devices listed for Uhi Corp. include CLINITRON AIR FLUIDIZED SUPPORT J-101UD, CLINITRON AIR FLUIDIZED SUPPORT SYSTEM and BARRIER BURN SHEET.