# Bontech, Inc.

- Location (FDA's records): Suwon-Si, KR
- FDA decisions: 5 (2016–2025): 5 510(k) clearances
- Names in FDA's records: Bontech, Inc. (3); Bontech Co., Ltd. (2)
- Product codes: MQB (4), IZL (1)
- 510(k) review time since 2016: median 37 days, against 92 for FDA's reviews in the same codes and years (1 of 5 faster)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 2 (2 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
- Remedi Co., Ltd.: 1 (https://510kreport.com/company/remedi)
- Samsung Mobile Display Co., Ltd.: 1 (https://510kreport.com/company/samsung-mobile-display)

## Its most-cited devices
- K162487: BSD3543 Digital Flat Panel X-ray Detector (2016), cited by 1
- K160204: BSD4343 Digital Flat Panel X-ray Detector (2016), cited by 1

## Recent decisions
- K243864: BONX805 (Sep 12, 2025)
- K200787: BSD3543W (Apr 23, 2020)
- K171485: BSD4343R Digital Flat Panel X-ray Detector (Jun 21, 2017)
- K162487: BSD3543 Digital Flat Panel X-ray Detector (Oct 14, 2016)
- K160204: BSD4343 Digital Flat Panel X-ray Detector (Jun 9, 2016)

Source page: https://510kreport.com/company/bontech