Resect Medical, Inc.
Country not established
- Devices
- 1
What Resect Medical, Inc. makes
Resect Medical, Inc. manufactures an inline bipolar radiofrequency (RF) linear coagulation device designed for surgical applications, specifically for precise tissue sealing and coagulation during procedures.
The company’s portfolio is regulated under Class II medical devices in the United States, with the device authorised via the FDA’s 510(k) clearance process. The manufacturer is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Resect Medical, Inc. have in the registry?
The registry currently lists 1 device for Resect Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Resect Medical, Inc.'s devices?
Among its 1 most recently registered device, Resect Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Resect Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Resect Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Resect Medical, Inc. in the registry?
The most recently registered devices listed for Resect Medical, Inc. include RESECT MEDICAL INLINE BI-POLAR RF LINEAR COAGULATION DEVICE.