Coviden, LLC
Country not established
- Devices
- 1
What Coviden, LLC makes
Coviden, LLC makes the Emprint SX Ablation Platform and its associated accessories, which are medical devices used for tissue ablation procedures.
The Emprint SX Ablation Platform and accessories are classified as Class II devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Emprint SX Ablation Platform and Accessories Ref K171358
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Coviden, LLC have in the registry?
The registry currently lists 1 device for Coviden, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Coviden, LLC's devices?
Among its 1 most recently registered device, Coviden, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Coviden, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Coviden, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Coviden, LLC in the registry?
The most recently registered devices listed for Coviden, LLC include Emprint SX Ablation Platform and Accessories.