Dynapulse Medical
Country not established
- Devices
- 1
What Dynapulse Medical makes
Dynapulse Medical manufactures the VEINOPLUS Back, a device designed for vein visualization and treatment, likely using imaging or therapeutic technologies for venous conditions.
The VEINOPLUS Back is classified as a Class II medical device and is listed under the FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
VEINOPLUS Back Ref K251958
510(k) 510(k)
Frequently asked questions
How many devices does Dynapulse Medical have in the registry?
The registry currently lists 1 device for Dynapulse Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dynapulse Medical's devices?
Among its 1 most recently registered device, Dynapulse Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Dynapulse Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dynapulse Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dynapulse Medical in the registry?
The most recently registered devices listed for Dynapulse Medical include VEINOPLUS Back.