Technolics, Inc.
Country not established
- Devices
- 1
What Technolics, Inc. makes
Technolics, Inc. manufactures bed-mounted patient monitoring devices designed for clinical use, enabling real-time observation of vital signs and patient status in hospital or care settings.
The company’s products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) clearance pathway. The portfolio is registered in the United States.
Catalogue
Monitor, Bed, Technolics Ref K770695
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Technolics, Inc. have in the registry?
The registry currently lists 1 device for Technolics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Technolics, Inc.'s devices?
Among its 1 most recently registered device, Technolics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Technolics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Technolics, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Technolics, Inc. in the registry?
The most recently registered devices listed for Technolics, Inc. include MONITOR, BED, TECHNOLICS.