Core-Vent Bio-Engineering, Inc.
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- Devices
- 1
What Core-Vent Bio-Engineering, Inc. makes
Core-Vent Bio-Engineering, Inc. manufactures the Paragon Implant System, a medical device designed for internal use in the human body.
The Paragon Implant System is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Paragon Implant System Ref K953101
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Core-Vent Bio-Engineering, Inc. have in the registry?
The registry currently lists 1 device for Core-Vent Bio-Engineering, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Core-Vent Bio-Engineering, Inc.'s devices?
Among its 1 most recently registered device, Core-Vent Bio-Engineering, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Core-Vent Bio-Engineering, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Core-Vent Bio-Engineering, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Core-Vent Bio-Engineering, Inc. in the registry?
The most recently registered devices listed for Core-Vent Bio-Engineering, Inc. include PARAGON IMPLANT SYSTEM.