Surx, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Surx, Inc. makes
Surx, Inc. manufactures radiofrequency electrosurgical generator systems and associated accessories, including the SURX LP System, the SURX TV System, and the SURX RF System.
These medical devices are classified as Class II and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Modification To Surx Radiofrequency Electrosurgical Generator System And Accessories (Surx Tv System) Ref K020126
Regimes: 510(k) Registry: 510(k)Surx Rf System Ref K020952
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surx, Inc. have in the registry?
The registry currently lists 3 devices for Surx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surx, Inc.'s devices?
Among its 3 most recently registered devices, Surx, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Surx, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Surx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surx, Inc. in the registry?
The most recently registered devices listed for Surx, Inc. include SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX LP SYSTEM), MODIFICATION TO SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX TV SYSTEM) and SURX RF SYSTEM.