Coviden (Formerly Registered AS US Surgical, A Div
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- Devices
- 1
What Coviden (Formerly Registered AS US Surgical, A Div makes
Coviden manufactures the SILS PORT, a single-incision laparoscopic port designed for minimally invasive surgical procedures, enabling access to the abdominal cavity through a small incision.
The SILS PORT is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Sils Port Ref K103253
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Coviden (Formerly Registered AS US Surgical, A Div have in the registry?
The registry currently lists 1 device for Coviden (Formerly Registered AS US Surgical, A Div. Devices recorded under merged duplicate company entries are counted once.
Which registries list Coviden (Formerly Registered AS US Surgical, A Div's devices?
Among its 1 most recently registered device, Coviden (Formerly Registered AS US Surgical, A Div has devices listed in FDA 510(k) (1 device).
What risk classes do Coviden (Formerly Registered AS US Surgical, A Div's devices fall under?
Among its 1 most recently registered device, the classes recorded for Coviden (Formerly Registered AS US Surgical, A Div's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Coviden (Formerly Registered AS US Surgical, A Div in the registry?
The most recently registered devices listed for Coviden (Formerly Registered AS US Surgical, A Div include SILS PORT.