Medical Device Manufacturer · KR , Anyang-Si, Gyeonggi-Do

Vericom Co., Ltd. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 2004

Recent clearances: Dual Core, Well-Root PT, MAZIC Claro CAD and MAZIC Claro Press

Total

Cleared

Denied

Vericom Co., Ltd. has 20 FDA 510(k) cleared dental devices. Based in Anyang-Si, Gyeonggi-Do, KR.

Latest FDA clearance: May 2026. Active since 2004.

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

510(k) submissions have been managed by LK Consulting Group USA, Inc. as regulatory consultant.

Vericom Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Vericom Co., Ltd.

20 devices

1-20 of 20

MAZIC Claro CAD and MAZIC Claro Press

K203672 · EIH

Dental · 197d

Cleared Aug 21, 2020

U-Cem Premium & MAZIC Cem

VONFLEX HEAVY, VINFLEX LIGHT

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: Jun 05, 2026

Vericom Co., Ltd. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Vericom Co., Ltd.

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