Convaid Product Development
Country not established
- Devices
- 1
What Convaid Product Development makes
Convaid Product Development manufactures therapy scooters designed for mobility assistance, including models for indoor and outdoor use. These devices support patients with limited mobility by providing a stable, maneuverable platform for short to moderate distances, often used in clinical or home settings.
The company’s therapy scooters fall under Class I regulatory classification in the US, requiring 510(k) clearance through the FDA. The devices are listed in the FDA’s 510(k) Premarket Notification Database. The manufacturer is based in the United States.
Catalogue
Therapy Scooter Ref K780296
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Convaid Product Development have in the registry?
The registry currently lists 1 device for Convaid Product Development. Devices recorded under merged duplicate company entries are counted once.
Which registries list Convaid Product Development's devices?
Among its 1 most recently registered device, Convaid Product Development has devices listed in FDA 510(k) (1 device).
What risk classes do Convaid Product Development's devices fall under?
Among its 1 most recently registered device, the classes recorded for Convaid Product Development's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Convaid Product Development in the registry?
The most recently registered devices listed for Convaid Product Development include THERAPY SCOOTER.