Proteus Biomedical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Proteus Biomedical, Inc. makes
Proteus Biomedical, Inc. manufactures the RAISIN Personal Monitor, a wearable device for continuous physiological monitoring, and the Proteus Ingestion Confirmation Systems, which verify medication intake via ingestible sensors.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Raisin Personal Monitor Ref K093976
Regimes: 510(k) Registry: 510(k)Proteus Ingestion Confinmation Systems Ref DEN120011
Regimes: De Novo Registry: De Novo
Frequently asked questions
How many devices does Proteus Biomedical, Inc. have in the registry?
The registry currently lists 2 devices for Proteus Biomedical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Proteus Biomedical, Inc.'s devices?
Among its 2 most recently registered devices, Proteus Biomedical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Proteus Biomedical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Proteus Biomedical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Proteus Biomedical, Inc. in the registry?
The most recently registered devices listed for Proteus Biomedical, Inc. include RAISIN PERSONAL MONITOR and PROTEUS INGESTION CONFINMATION SYSTEMS.