Cogent
Country not established
- Devices
- 1
What Cogent makes
Cogent manufactures PARIETEX, a surgical mesh product designed for hernia repair and abdominal wall reconstruction, intended to provide durable reinforcement of soft tissue.
The company’s portfolio is regulated under FDA Class II devices, with PARIETEX listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Parietex Ref K982532
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cogent have in the registry?
The registry currently lists 1 device for Cogent. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cogent's devices?
Among its 1 most recently registered device, Cogent has devices listed in FDA 510(k) (1 device).
What risk classes do Cogent's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cogent's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cogent in the registry?
The most recently registered devices listed for Cogent include PARIETEX.