Radiance Therapeutics, Inc.
Country not established
- Devices
- 1
What Radiance Therapeutics, Inc. makes
Radiance Therapeutics, Inc. manufactures the RadianceTx Radionuclide Brachytherapy Source, a device used for targeted radiation treatment in medical procedures. This source is designed for precise delivery of radiation to specific tissue areas, commonly applied in oncology for localized tumor treatment.
The company’s product portfolio is classified under FDA Class II devices and is subject to 510(k) clearance requirements in the United States. The Radionuclide Brachytherapy Source is listed in the FDA’s 510(k) registry, adhering to regulatory standards for radiation-emitting devices.
Catalogue
RadianceTx Radionuclide Brachytherapy Source Ref K223465
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Radiance Therapeutics, Inc. have in the registry?
The registry currently lists 1 device for Radiance Therapeutics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Radiance Therapeutics, Inc.'s devices?
Among its 1 most recently registered device, Radiance Therapeutics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Radiance Therapeutics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Radiance Therapeutics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Radiance Therapeutics, Inc. in the registry?
The most recently registered devices listed for Radiance Therapeutics, Inc. include RadianceTx Radionuclide Brachytherapy Source.