Medical Device Manufacturer · KR , Seul

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

2 submissions · 2 cleared · Since 2005

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Acucera, Inc. Dental ✕

2 devices

1-2 of 2

Cleared Mar 26, 2007

ZIRBLANK-PS AND ZIRBLANK-FS

Cleared Oct 19, 2005

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Apr 28, 2026