Medical Device Manufacturer · US , Encino , CA

Core-Vent Corp. - FDA 510(k) Cleared Devices

25 submissions · 25 cleared · Since 1986

Total

Cleared

Denied

Core-Vent Corp. has 25 FDA 510(k) cleared dental devices. Based in Encino, US.

Historical record: 25 cleared submissions from 1986 to 2000.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Core-Vent Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Core-Vent Corp.

25 devices

1-12 of 25

Cleared Dec 08, 2000

ADVENT IMPLANT SYSTEM

K002614 · DZE

Dental · 108d

Cleared Oct 30, 2000

SWISSPLUS IMPLANT SYSTEM, MODEL SPWB 8,10,12,14/OPH20/SMPR, SPB...

TSIR ANGLED ABUTMENTS

K910585 · DZE

Dental · 235d

Cleared May 15, 1991

BIO-VENT-X ENDOSSEOUS HA COATED DENTAL IMPLANTS

K902968 · DZE

Dental · 313d

Cleared Feb 20, 1991

SCREW-VENT ENDOSSEOUS IMPLANT ABUTMENTS

K900179 · DZE

Dental · 400d

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 27, 2026

Core-Vent Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Core-Vent Corp.

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