Genetic
Country not established
- Devices
- 1
What Genetic makes
Genetic manufactures the PERI-GUARD pericardial patch, a surgical mesh device designed for hernia repair within the pericardial space.
The device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Peri-Guard Pericardial Patch-Hernia Ref K833021
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Genetic have in the registry?
The registry currently lists 1 device for Genetic. Devices recorded under merged duplicate company entries are counted once.
Which registries list Genetic's devices?
Among its 1 most recently registered device, Genetic has devices listed in FDA 510(k) (1 device).
What risk classes do Genetic's devices fall under?
Among its 1 most recently registered device, the classes recorded for Genetic's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Genetic in the registry?
The most recently registered devices listed for Genetic include PERI-GUARD PERICARDIAL PATCH-HERNIA.