Dermanetics Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Dermanetics Corp. makes
Dermanetics Corp. manufactures medical waterbed systems, including the SYSTEM 2500 and SYSTEM 3000, which incorporate fluidized air technology for patient support and mobility.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
System 2500 Medical Waterbed Ref K894723
Regimes: 510(k) Registry: 510(k)System 3000 Fluidized Air Bed Ref K890935
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dermanetics Corp. have in the registry?
The registry currently lists 2 devices for Dermanetics Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dermanetics Corp.'s devices?
Among its 2 most recently registered devices, Dermanetics Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Dermanetics Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dermanetics Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dermanetics Corp. in the registry?
The most recently registered devices listed for Dermanetics Corp. include SYSTEM 2500 MEDICAL WATERBED and SYSTEM 3000 FLUIDIZED AIR BED.