Medical Device Manufacturer · KR , Yongin-Si

Vatech Acucera, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2021

Total

Cleared

Denied

Vatech Acucera, Inc. has 4 FDA 510(k) cleared medical devices. Based in Yongin-Si, KR.

Last cleared in 2022. Active since 2021. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Vatech Acucera, Inc. Filter by specialty or product code using the sidebar.

Vatech Acucera, Inc. 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 - Vatech Acucera, Inc.

4 devices

1-4 of 4