Ali-Oop Co., Inc.
Country not established
- Devices
- 1
What Ali-Oop Co., Inc. makes
Ali-Oop Co., Inc. manufactures a device designed for repositioning patients who are lying down, likely used in clinical or hospital settings to adjust patient positioning during treatment or recovery.
The company’s portfolio is regulated under FDA Class I devices, with products listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Device For Repositioning A Bet Patient Ref K813356
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ali-Oop Co., Inc. have in the registry?
The registry currently lists 1 device for Ali-Oop Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ali-Oop Co., Inc.'s devices?
Among its 1 most recently registered device, Ali-Oop Co., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ali-Oop Co., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ali-Oop Co., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ali-Oop Co., Inc. in the registry?
The most recently registered devices listed for Ali-Oop Co., Inc. include DEVICE FOR REPOSITIONING A BET PATIENT.