Lydus Medical, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Lydus Medical, Ltd. makes
Lydus Medical, Ltd. manufactures the Vesseal, a surgical device designed for vascular anastomosis closure, intended to reduce bleeding and improve surgical outcomes during procedures involving blood vessels.
The Vesseal 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
Vesseal Ref K221280
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lydus Medical, Ltd. have in the registry?
The registry currently lists 1 device for Lydus Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lydus Medical, Ltd.'s devices?
Among its 1 most recently registered device, Lydus Medical, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Lydus Medical, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lydus Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lydus Medical, Ltd. in the registry?
The most recently registered devices listed for Lydus Medical, Ltd. include Vesseal.