# Surgident

- Location (FDA's records): Seongnam-Si, KR
- FDA decisions: 2 (2018–2019): 2 510(k) clearances
- Names in FDA's records: Surgident (1); Surgident Co., Ltd. (1)
- Product codes: JEY (1), NHA (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 2 (0 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
- Impladent, Ltd.: 1 (https://510kreport.com/company/impladent)
- Jeil Medical Corporation: 1 (https://510kreport.com/company/jeil-medical)
- Medimecca Co., Ltd.: 1 (https://510kreport.com/company/medimecca)

## Firms that cite its devices most
- Montjade Engineering Co., Ltd.: 1 (https://510kreport.com/company/montjade-engineering)
- Dentis Co., Ltd.: 1 (https://510kreport.com/company/dentis)

## Its most-cited devices
- K170697: GBR system (2018), cited by 2

## Recent decisions
- K173570: SD Abutment (May 17, 2019)
- K170697: GBR system (May 24, 2018)

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