Wesper, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
What Wesper, Inc. makes
Wesper, Inc. makes the Wesper Lab, CASSIE, and WesperO2 devices.
These devices are Class II medical devices listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Wesper Lab Ref K203343
Regimes: 510(k) Registry: 510(k)Cassie Ref K252628
Regimes: 510(k) Registry: 510(k)Wesper Lab Ref K221816
Regimes: 510(k) Registry: 510(k)WesperO2 Ref K213515
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 081210033
- [email protected]
- Phone
- 9175400177
Frequently asked questions
How many devices does Wesper, Inc. have in the registry?
The registry currently lists 7 devices for Wesper, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wesper, Inc.'s devices?
Among its 7 most recently registered devices, Wesper, Inc. has devices listed in FDA 510(k) (4 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Wesper, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Wesper, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wesper, Inc. in the registry?
The most recently registered devices listed for Wesper, Inc. include CASSIE 0.9.0, Wesper Lab WSWW-RE-K-N-V01-GRD, Wesper Lab WSWW-RE-K-N-V02-BLO and Wesper Lab.