Ensite Vacular, LLC
Country not established
- Devices
- 1
What Ensite Vacular, LLC makes
Ensite Vascular, LLC manufactures the SiteSeal Femoral Compression Device, a medical device designed for vascular access site management, specifically to apply compression to femoral artery puncture sites to reduce bleeding risk during or after procedures.
The SiteSeal Femoral Compression Device is classified as a Class II medical device in the US and is authorised through the FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
SiteSeal Femoral Compression Device Ref K192413
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ensite Vacular, LLC have in the registry?
The registry currently lists 1 device for Ensite Vacular, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ensite Vacular, LLC's devices?
Among its 1 most recently registered device, Ensite Vacular, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Ensite Vacular, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ensite Vacular, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ensite Vacular, LLC in the registry?
The most recently registered devices listed for Ensite Vacular, LLC include SiteSeal Femoral Compression Device.