Endoprime, Inc.
Country not established
- Devices
- 1
What Endoprime, Inc. makes
Endoprime, Inc. manufactures the Prime Adaptive Ultrasonic Scalpel System, a device designed for precise tissue dissection and coagulation using ultrasonic energy in surgical procedures.
The company’s portfolio is regulated under FDA Class II (U) devices and is listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Prime Adaptive Ultrasonic Scalpel System Ref K150271
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endoprime, Inc. have in the registry?
The registry currently lists 1 device for Endoprime, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endoprime, Inc.'s devices?
Among its 1 most recently registered device, Endoprime, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Endoprime, Inc. in the registry?
The most recently registered devices listed for Endoprime, Inc. include Prime Adaptive Ultrasonic Scalpel System.