Radtec Medical Devices, Inc.
Country not established
- Devices
- 1
What Radtec Medical Devices, Inc. makes
Radtec Medical Devices, Inc. manufactures the Lollipop BiteBlock, a device designed to prevent biting during medical procedures, particularly for pediatric or vulnerable patients.
The Lollipop BiteBlock is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Lollipop BiteBlock Ref K200652
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Radtec Medical Devices, Inc. have in the registry?
The registry currently lists 1 device for Radtec Medical Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Radtec Medical Devices, Inc.'s devices?
Among its 1 most recently registered device, Radtec Medical Devices, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Radtec Medical Devices, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Radtec Medical Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Radtec Medical Devices, Inc. in the registry?
The most recently registered devices listed for Radtec Medical Devices, Inc. include Lollipop BiteBlock.