Proactive Comfort, LLC
United Statesfrom the FDA registration address FDA establishment FEI 3021027216
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pure Tilt Ref K152021
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3021027216
- Address
- 3901 Centerview Dr Ste L, Chantilly, VA, 20151
Frequently asked questions
How many devices does PROACTIVE COMFORT, LLC have in the registry?
The registry currently lists 1 device for PROACTIVE COMFORT, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list PROACTIVE COMFORT, LLC's devices?
Among its 1 most recently registered device, PROACTIVE COMFORT, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do PROACTIVE COMFORT, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for PROACTIVE COMFORT, LLC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from PROACTIVE COMFORT, LLC in the registry?
The most recently registered devices listed for PROACTIVE COMFORT, LLC include Pure Tilt.