Jet Soft Srl
RomaniaFDA 510(k) applicant, unverified
- Devices
- 1
Catalogue
Biojet Ref K122329
What Jet Soft Srl makes
Jet Soft Srl manufactures the BIOJET, a medical device designed for soft tissue treatment and regeneration, likely used in orthopedic or sports medicine applications.
The BIOJET is classified as a Class II device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Frequently asked questions
How many devices does Jet Soft Srl have in the registry?
The registry currently lists 1 device for Jet Soft Srl. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jet Soft Srl's devices?
Among its 1 most recently registered device, Jet Soft Srl has devices listed in FDA 510(k) (1 device).
What risk classes do Jet Soft Srl's devices fall under?
Among its 1 most recently registered device, the classes recorded for Jet Soft Srl's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jet Soft Srl in the registry?
The most recently registered devices listed for Jet Soft Srl include BIOJET.