Oceanside Biomedics
Country not established
- Devices
- 1
What Oceanside Biomedics makes
Oceanside Biomedics manufactures cannula and trocar devices, which are used in minimally invasive surgical procedures to create access ports in tissue.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Cannula And Trocar Ref K912836
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oceanside Biomedics have in the registry?
The registry currently lists 1 device for Oceanside Biomedics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oceanside Biomedics's devices?
Among its 1 most recently registered device, Oceanside Biomedics has devices listed in FDA 510(k) (1 device).
What risk classes do Oceanside Biomedics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Oceanside Biomedics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oceanside Biomedics in the registry?
The most recently registered devices listed for Oceanside Biomedics include CANNULA AND TROCAR.