Life Outcomes, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Life Outcomes, Inc. makes
Life Outcomes, Inc. manufactures the DPILOG (Model DPC-512), a device designed for digital pressure injury logging and monitoring to track wound progression and treatment responses.
The company’s portfolio is regulated under FDA’s Class II device classification and is listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Regimes: 510(k) Registry: 510(k)
Dpilog, Model Dpc-512 Ref K062811
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Life Outcomes, Inc. have in the registry?
The registry currently lists 6 devices for Life Outcomes, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Life Outcomes, Inc.'s devices?
Among its 6 most recently registered devices, Life Outcomes, Inc. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Life Outcomes, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Life Outcomes, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Life Outcomes, Inc. in the registry?
The most recently registered devices listed for Life Outcomes, Inc. include C-Quest 40-200, C-Quest 40-250-PR-UT, C-Quest 40-250-PR and C-Quest 40-200-21A.