Human Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Human Technologies, Inc. makes
Human Technologies, Inc. manufactures remote patient monitoring devices, including a wireless actuator for medical interventions, a bed-based presence sensor for patient tracking, and a swallowable temperature-monitoring system for internal body temperature tracking.
The company’s products are regulated under FDA 510(k) clearance, with devices classified as Class I and Class II. They are listed in the FDA’s 510(k) database and are based in the United States.
Catalogue
Sibis Remote Actuator Ref K871158
Regimes: 510(k) Registry: 510(k)Bed Patient Presence Monitor Ref K871203
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Human Technologies, Inc. have in the registry?
The registry currently lists 3 devices for Human Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Human Technologies, Inc.'s devices?
Among its 3 most recently registered devices, Human Technologies, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Human Technologies, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Human Technologies, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Human Technologies, Inc. in the registry?
The most recently registered devices listed for Human Technologies, Inc. include SIBIS REMOTE ACTUATOR, BED PATIENT PRESENCE MONITOR and ACCUTEMP(TM) TEMP. MONITIORING SYSTEM SWALLOWABLE.