Permobil of America
Country not established
- Devices
- 5
What Permobil of America makes
Permobil of America manufactures a range of manual and lightweight electric wheelchairs, including the Exterior (outdoor-focused), Minior (compact), Hexior (foldable), Superior (standard electric), and Maxior (heavy-duty). These devices are designed for indoor and outdoor mobility, with features tailored to different user needs such as portability, durability, and maneuverability.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. These devices are listed in the FDA’s 510(k) database, reflecting their compliance with U.S. medical device authorization requirements. The manufacturer operates from the United States.
Catalogue
Permobil Exterior Ref K870225
Regimes: 510(k) Registry: 510(k)Permobil Minior Ref K870226
Regimes: 510(k) Registry: 510(k)Permobil Hexior Ref K870228
Regimes: 510(k) Registry: 510(k)Permobil Superior Ref K870227
Regimes: 510(k) Registry: 510(k)Permobil Maxior Ref K870224
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Permobil of America have in the registry?
The registry currently lists 5 devices for Permobil of America. Devices recorded under merged duplicate company entries are counted once.
Which registries list Permobil of America's devices?
Among its 5 most recently registered devices, Permobil of America has devices listed in FDA 510(k) (5 devices).
What risk classes do Permobil of America's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Permobil of America's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Permobil of America in the registry?
The most recently registered devices listed for Permobil of America include PERMOBIL EXTERIOR, PERMOBIL MINIOR, PERMOBIL HEXIOR and PERMOBIL SUPERIOR.