Surcraft, LLC
Country not established
- Devices
- 1
What Surcraft, LLC makes
Surcraft, LLC manufactures the SOLO BAND LIGATOR, a device used for surgical ligation, designed to securely apply and cut bands on tissue or vessels during procedures.
The SOLO BAND LIGATOR is classified as a Class II medical device under FDA regulations and is listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Solo Band Ligator Ref K960020
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surcraft, LLC have in the registry?
The registry currently lists 1 device for Surcraft, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surcraft, LLC's devices?
Among its 1 most recently registered device, Surcraft, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Surcraft, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Surcraft, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surcraft, LLC in the registry?
The most recently registered devices listed for Surcraft, LLC include SOLO BAND LIGATOR.