American Surgical Devices
Country not established
- Devices
- 1
What American Surgical Devices makes
American Surgical Devices manufactures the A.S.D. SAFETY TROCAR, a surgical instrument designed for minimally invasive procedures to create access ports in tissue while reducing risks of injury during insertion.
The company’s trocar is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) clearance process. The product is regulated under US jurisdiction.
Catalogue
A.S.D. Safety Trocar Ref K955412
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Surgical Devices have in the registry?
The registry currently lists 1 device for American Surgical Devices. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Surgical Devices's devices?
Among its 1 most recently registered device, American Surgical Devices has devices listed in FDA 510(k) (1 device).
What risk classes do American Surgical Devices's devices fall under?
Among its 1 most recently registered device, the classes recorded for American Surgical Devices's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Surgical Devices in the registry?
The most recently registered devices listed for American Surgical Devices include A.S.D. SAFETY TROCAR.