Alive, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Alive, Inc. makes
Alive, Inc. manufactures electromedical devices for wound care and drainage, including the HAKOMED ELECDT/VACUPULLS and the HAKOMED ELECDT/PRO ELEDT series. These products are designed for vacuum-assisted wound therapy and electrical stimulation applications.
The company’s portfolio is regulated under FDA Class II devices, with relevant products listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Hakomed Elecdt/Vacupulls Ref K980958
Regimes: 510(k) Registry: 510(k)Hakomed Elecdt / Pro Eledt Series Ref K980892
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alive, Inc. have in the registry?
The registry currently lists 2 devices for Alive, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alive, Inc.'s devices?
Among its 2 most recently registered devices, Alive, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Alive, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Alive, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alive, Inc. in the registry?
The most recently registered devices listed for Alive, Inc. include HAKOMED ELECDT/VACUPULLS and HAKOMED ELECDT / PRO ELEDT SERIES.