Power Plus Mobility
CanadaFDA applicant, unverified FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Power Plus Mobility makes
Power Plus Mobility manufactures the SuperTilt Plus (STP), a manual wheelchair tilt mechanism designed to adjust the seating position for improved user comfort and pressure distribution. This device is intended for use in clinical and home settings to enhance mobility and reduce the risk of pressure ulcers for wheelchair-dependent individuals.
The SuperTilt Plus is classified as a Class I medical device under FDA regulations and has been authorised through the 510(k) clearance process. The company operates from the United States, where its products are listed in the FDA’s regulatory database.
Catalogue
Supertilt Plus (Stp) Ref K221435
Regimes: 510(k) Registry: 510(k)
FDA establishments
- Power Plus Mobility Inc Guelph Ontario · CA FEI 3023141620
Frequently asked questions
How many devices does Power Plus Mobility have in the registry?
The registry currently lists 1 device for Power Plus Mobility. Devices recorded under merged duplicate company entries are counted once.
Which registries list Power Plus Mobility's devices?
Among its 1 most recently registered device, Power Plus Mobility has devices listed in FDA 510(k) (1 device).
What risk classes do Power Plus Mobility's devices fall under?
Among its 1 most recently registered device, the classes recorded for Power Plus Mobility's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Power Plus Mobility in the registry?
The most recently registered devices listed for Power Plus Mobility include SUPERTILT PLUS (STP).
Which FDA establishments are linked to Power Plus Mobility?
1 FDA establishment is linked to Power Plus Mobility in the registry; they are listed on the company page.