Rdm Intl., Inc.
Country not established
- Devices
- 1
What Rdm Intl., Inc. makes
Rdm Intl., Inc. manufactures the Thermosurgery™ device, a system designed for controlled thermal ablation procedures in medical settings.
The Thermosurgery™ device is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Thermosurgery Tm Ref K894166
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rdm Intl., Inc. have in the registry?
The registry currently lists 1 device for Rdm Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rdm Intl., Inc.'s devices?
Among its 1 most recently registered device, Rdm Intl., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Rdm Intl., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Rdm Intl., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rdm Intl., Inc. in the registry?
The most recently registered devices listed for Rdm Intl., Inc. include THERMOSURGERY TM.