Hemostace, LLC
Country not established
- Devices
- 1
What Hemostace, LLC makes
Hemostace, LLC manufactures the SORBASTACE, a surgical device designed for rapid hemostasis during procedures requiring precise blood control.
The SORBASTACE is classified as a Class II (U) device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Sorbastace Ref K965034
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hemostace, LLC have in the registry?
The registry currently lists 1 device for Hemostace, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hemostace, LLC's devices?
Among its 1 most recently registered device, Hemostace, LLC has devices listed in FDA 510(k) (1 device).
What are the newest devices from Hemostace, LLC in the registry?
The most recently registered devices listed for Hemostace, LLC include SORBASTACE.