Corsens Medical, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Corsens Medical, Ltd. makes
Corsens Medical, Ltd. manufactures the CorSens, a medical device designed for use in cardiac rhythm management, specifically as a leadless pacemaker for patients requiring single-chamber pacing.
The CorSens device 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
CorSens Ref K160656
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Corsens Medical, Ltd. have in the registry?
The registry currently lists 1 device for Corsens Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Corsens Medical, Ltd.'s devices?
Among its 1 most recently registered device, Corsens Medical, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Corsens Medical, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Corsens Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Corsens Medical, Ltd. in the registry?
The most recently registered devices listed for Corsens Medical, Ltd. include CorSens.