Stryker Canada
CanadaFDA applicant, unverified
- Devices
- 1
What Stryker Canada makes
Stryker Canada manufactures the Stryker Sorano wheelchair, a mobility aid designed for users requiring manual or electric propulsion with adjustable features for comfort and accessibility.
The Sorano wheelchair is classified as a Class I medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Syryker Sorano Wheelchair Ref K051369
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stryker Canada have in the registry?
The registry currently lists 1 device for Stryker Canada. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stryker Canada's devices?
Among its 1 most recently registered device, Stryker Canada has devices listed in FDA 510(k) (1 device).
What risk classes do Stryker Canada's devices fall under?
Among its 1 most recently registered device, the classes recorded for Stryker Canada's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Stryker Canada in the registry?
The most recently registered devices listed for Stryker Canada include SYRYKER SORANO WHEELCHAIR.