LifeLens Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
LifeLens Physiological Monitor Ref K260157
Regimes: 510(k) Registry: 510(k)LifeLens Wireless ECG Monitor Ref K203168
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does LifeLens Technologies, Inc. have in the registry?
The registry currently lists 2 devices for LifeLens Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list LifeLens Technologies, Inc.'s devices?
Among its 2 most recently registered devices, LifeLens Technologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do LifeLens Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for LifeLens Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from LifeLens Technologies, Inc. in the registry?
The most recently registered devices listed for LifeLens Technologies, Inc. include LifeLens Physiological Monitor and LifeLens Wireless ECG Monitor.