Ken Kemmerer
Country not established
- Devices
- 2
What Ken Kemmerer makes
Ken Kemmerer manufactures patient mobility devices, including electric-powered patient lifts and seat lift chairs designed for clinical and home care settings. These products assist in transferring and repositioning patients with limited mobility, reducing caregiver strain.
The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) pathway. These devices are based in the United States and appear in the FDA’s 510(k) clearance registry.
Catalogue
A.C. Power Patient Lift Ref K935351
Regimes: 510(k) Registry: 510(k)Electric Seat Lift Chair Ref K961663
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ken Kemmerer have in the registry?
The registry currently lists 2 devices for Ken Kemmerer. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ken Kemmerer's devices?
Among its 2 most recently registered devices, Ken Kemmerer has devices listed in FDA 510(k) (2 devices).
What risk classes do Ken Kemmerer's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ken Kemmerer's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ken Kemmerer in the registry?
The most recently registered devices listed for Ken Kemmerer include A.C. POWER PATIENT LIFT and ELECTRIC SEAT LIFT CHAIR.