# S&G Biotech, Inc.

- Location (FDA's records): Yongin-Si, KR
- FDA decisions: 2 (2023–2025): 2 510(k) clearances
- Product codes: FGE (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (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
- M.I.Tech Co., Ltd.: 1 (https://510kreport.com/company/mitech)

## Its most-cited devices
- K223354: EGIS Biliary Single Bare Stent (2023), cited by 1

## Recent decisions
- K242845: EGIS Biliary Double Bare Stent (BDB080405) (Jun 25, 2025)
- K223354: EGIS Biliary Single Bare Stent (Sep 21, 2023)

Source page: https://510kreport.com/company/s-g-biotech