Wearlinq, Inc.
Country not established
- Devices
- 4
What Wearlinq, Inc. makes
Wearlinq, Inc. manufactures the eWave Monitor, a device designed for continuous, non-invasive monitoring of physiological signals, such as heart rate and rhythm, for patient assessment and remote health tracking.
The eWave Monitor is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) premarket notification process. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
eWave Monitor Ref K214073
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 144863125
- [email protected]
- Phone
- 1-800-785-4354
Frequently asked questions
How many devices does Wearlinq, Inc. have in the registry?
The registry currently lists 4 devices for Wearlinq, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wearlinq, Inc.'s devices?
Among its 4 most recently registered devices, Wearlinq, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Wearlinq, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Wearlinq, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wearlinq, Inc. in the registry?
The most recently registered devices listed for Wearlinq, Inc. include eWave 6-Lead EKG, eWave Electrode Patch and eWave Monitor.