# BLUECORE COMPANY Co., Ltd.

- Location (FDA's records): Busan, KR
- FDA decisions: 4 (2017–2026): 4 510(k) clearances
- Names in FDA's records: BLUECORE COMPANY Co., Ltd. (3); Bluecore Co., Ltd. (1)
- Product codes: GEX (4)
- 510(k) review time since 2016: median 145 days, against 90 for FDA's reviews in the same codes and years (0 of 4 faster)
- Predicates its devices cite: 5 (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
- Lutronic Corporation: 1 (https://510kreport.com/company/lutronic)
- Alma Lasers, Inc.: 1 (https://510kreport.com/company/alma-lasers)
- Quanta System Spa: 1 (https://510kreport.com/company/quanta-system)
- Cutera, Inc.: 1 (https://510kreport.com/company/cutera)
- Cynosure, Inc.: 1 (https://510kreport.com/company/cynosure)

## Firms that cite its devices most
- Bio-Med USA, Inc.: 2 (https://510kreport.com/company/bio-med-usa)

## Its most-cited devices
- K171648: BM.Iris (2017), cited by 2

## Recent decisions
- K254199: PicoreMax (PicoreMax) (Sep 24, 2026)
- K241951: Lasya-Trinity (Oct 10, 2024)
- K230268: ZenPro 40 (Aug 10, 2023)
- K171648: BM.Iris (Sep 8, 2017)

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