Scion International, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Scion International, Inc. makes
Scion International, Inc. manufactures vascular surgical clips, including titanium DUOCLIPPER clips for vessel occlusion, and tools for saphenous vein harvesting such as the SCION Balloon Elevator and the SCION Saphenous Vein Harvesting System. The company also produces the RABBIT device, designed for specific vascular procedures.
The company’s products are regulated under FDA 510(k) clearance, with devices classified as Class I and Class II. These products are listed in the FDA’s 510(k) database. Scion International, Inc. is based in the United States.
Catalogue
Duoclipper Titanium Clips Ref K973652
Regimes: 510(k) Registry: 510(k)Scion Saphenous Vein Harvesting System Ref K963006
Regimes: 510(k) Registry: 510(k)Rabbit Ref K040087
Regimes: 510(k) Registry: 510(k)Scion Balloon Elevator Ref K973698
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Scion International, Inc. have in the registry?
The registry currently lists 4 devices for Scion International, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Scion International, Inc.'s devices?
Among its 4 most recently registered devices, Scion International, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Scion International, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Scion International, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Scion International, Inc. in the registry?
The most recently registered devices listed for Scion International, Inc. include DUOCLIPPER TITANIUM CLIPS, SCION SAPHENOUS VEIN HARVESTING SYSTEM, RABBIT and SCION BALLOON ELEVATOR.