Vent Creativity
United Statesfrom the FDA registration address FDA FEI 3045521711
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Vent Creativity Knee v1.0 (Hermes) Ref K241961
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3045521711
- Address
- 12 E 49th St Fl 11, New York, NY, 10017
Frequently asked questions
How many devices does Vent Creativity have in the registry?
The registry currently lists 1 device for Vent Creativity. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vent Creativity's devices?
Among its 1 most recently registered device, Vent Creativity has devices listed in FDA 510(k) (1 device).
What risk classes do Vent Creativity's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vent Creativity's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vent Creativity in the registry?
The most recently registered devices listed for Vent Creativity include Vent Creativity Knee v1.0 (Hermes).