Gsi Development Co.
Country not established
- Devices
- 4
What Gsi Development Co. makes
Gsi Development Co. manufactures fluidized air bed systems, including the MicroAir 3500, MicroAir Turn-Q, and MicroAir Fluidized Air Bed. These devices are designed for patient positioning and support in clinical settings, reducing pressure points and improving mobility for immobilized patients.
The company’s portfolio is regulated under Class II medical devices in the US, with devices listed via the FDA’s 510(k) pathway. Products are included in the FDA’s regulatory registry for clearance and post-market surveillance.
Catalogue
Fluidized Air Bed Ref K893708
Regimes: 510(k) Registry: 510(k)Microair 3500 Ref K914674
Regimes: 510(k) Registry: 510(k)Microair Turn-Q Ref K926456
Regimes: 510(k) Registry: 510(k)Microair Fluidized Air Bed Ref K884529
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gsi Development Co. have in the registry?
The registry currently lists 4 devices for Gsi Development Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gsi Development Co.'s devices?
Among its 4 most recently registered devices, Gsi Development Co. has devices listed in FDA 510(k) (4 devices).
What risk classes do Gsi Development Co.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Gsi Development Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gsi Development Co. in the registry?
The most recently registered devices listed for Gsi Development Co. include FLUIDIZED AIR BED, MICROAIR 3500, MICROAIR TURN-Q and MICROAIR FLUIDIZED AIR BED.