Core-Vent Corp.
United StatesFDA applicant, unverified
- Devices
- 25
What Core-Vent Corp. makes
Core-Vent Corp. manufactures dental implants and abutment systems, including endosseous implants with hydroxyapatite (HA) coatings, pre-angled abutments, and screw-vent designs for bone integration. Their portfolio includes blade and screw-type implants, such as the Sub-Vent™ and Screw-Vent implants, as well as specialized systems like the Advent Implant System and Micro-Vent/HA for precise dental restoration.
The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory clearance via the 510(k) pathway. Products are listed in the FDA’s 510(k) registry, and the manufacturer operates from the United States.
Catalogue
Search and filter all 25 devicesFrequently asked questions
How many devices does Core-Vent Corp. have in the registry?
The registry currently lists 25 devices for Core-Vent Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Core-Vent Corp.'s devices?
Among its 25 most recently registered devices, Core-Vent Corp. has devices listed in FDA 510(k) (25 devices).
What risk classes do Core-Vent Corp.'s devices fall under?
Among its 25 most recently registered devices, the classes recorded for Core-Vent Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Core-Vent Corp. in the registry?
The most recently registered devices listed for Core-Vent Corp. include SCREW-VENT IMPLANT, SUB-VENT (TM) IMPLANT/ENDOSSEOUS BLADE IMPLANT, BIO-VENT IMPLANT and PRE-ANGLED ABUTMENTS.