Nanowear, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Nanowear, Inc. makes
Nanowear, Inc. makes the SimpleSENSE Platform, which includes devices such as SimplECG, SimpleSENSE, and SimpleSense-BP along with its associated software application.
These devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
SimpleSENSE Platform Ref K212160
Regimes: 510(k) Registry: 510(k)SimplECG Ref K161431
Regimes: 510(k) Registry: 510(k)SimpleSENSE Ref K201669
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nanowear, Inc. have in the registry?
The registry currently lists 4 devices for Nanowear, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nanowear, Inc.'s devices?
Among its 4 most recently registered devices, Nanowear, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Nanowear, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Nanowear, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nanowear, Inc. in the registry?
The most recently registered devices listed for Nanowear, Inc. include SimpleSENSE Platform, SimplECG, SimpleSENSE and SimpleSense-BP, SimpleSense-BP Software Application.