Technology 2000
Country not established
- Devices
- 1
What Technology 2000 makes
Technology 2000 manufactures the HEMOR-ICE, a device designed for hemostasis in surgical procedures, particularly for controlling bleeding in vascular or soft tissue applications.
The HEMOR-ICE 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
Hemor-Ice Ref K854569
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Technology 2000 have in the registry?
The registry currently lists 1 device for Technology 2000. Devices recorded under merged duplicate company entries are counted once.
Which registries list Technology 2000's devices?
Among its 1 most recently registered device, Technology 2000 has devices listed in FDA 510(k) (1 device).
What are the newest devices from Technology 2000 in the registry?
The most recently registered devices listed for Technology 2000 include HEMOR-ICE.