Henry Enterprises, Inc.
Country not established
- Devices
- 1
What Henry Enterprises, Inc. makes
Henry Enterprises, Inc. manufactures the LIFT MASTER PATIENT LIFT, a device designed for transferring and repositioning patients who require mobility assistance, particularly in clinical or home care settings.
The LIFT MASTER PATIENT LIFT is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Lift Master Patient Lift Ref K896848
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Henry Enterprises, Inc. have in the registry?
The registry currently lists 1 device for Henry Enterprises, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Henry Enterprises, Inc.'s devices?
Among its 1 most recently registered device, Henry Enterprises, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Henry Enterprises, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Henry Enterprises, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Henry Enterprises, Inc. in the registry?
The most recently registered devices listed for Henry Enterprises, Inc. include LIFT MASTER PATIENT LIFT.