# Vatech Acucera, Inc.

- Location (FDA's records): Yongin-Si, KR
- FDA decisions: 4 (2021–2022): 4 510(k) clearances
- Product codes: EIH (4)
- 510(k) review time since 2016: median 122 days, against 131 for FDA's reviews in the same codes and years (3 of 4 faster)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Liaoning Upcera Co., Ltd.: 3 (https://510kreport.com/company/liaoning-upcera)

## Firms that cite its devices most
- Prismatik Dentalcraft, Inc.: 1 (https://510kreport.com/company/prismatik-dentalcraft)

## Its most-cited devices
- K203590: Perfit FS Dental Zirconia Fully Sintered Block (2021), cited by 2

## Recent decisions
- K222686: Perfit FS Dental Zirconia Fully Sintered Block (Oct 6, 2022)
- K203590: Perfit FS Dental Zirconia Fully Sintered Block (Jun 24, 2021)
- K203499: Perfit ZR ST Dental Zirconia blank, Perfit ZR UT Dental Zirconia blank (Apr 5, 2021)
- K203351: Perfit ZR HT Dental Zirconia blank (Mar 8, 2021)

Source page: https://510kreport.com/company/vatech-acucera