Comfort Acrylics, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 1000125917
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
What Comfort Acrylics, Inc. makes
Comfort Acrylics, Inc. makes the SleepApp device.
The SleepApp device is a Class II medical device listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Comfor-Dent Denture Liner Ref K910795
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Sleepapp Ref K182202
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000125917
- Address
- 2103 N.E. 272ND AVE., CAMAS, WA, 98607
Frequently asked questions
How many devices does COMFORT ACRYLICS, INC. have in the registry?
The registry currently lists 3 devices for COMFORT ACRYLICS, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list COMFORT ACRYLICS, INC.'s devices?
Among its 3 most recently registered devices, COMFORT ACRYLICS, INC. has devices listed in FDA 510(k) (3 devices).
What risk classes do COMFORT ACRYLICS, INC.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for COMFORT ACRYLICS, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from COMFORT ACRYLICS, INC. in the registry?
The most recently registered devices listed for COMFORT ACRYLICS, INC. include COMFOR-DENT DENTURE LINER, COMFORT ACRYLICS PLIABLE DENTURE LINERS & SPLINTS and SLEEPAPP.