# Meta Systems Co., Ltd.

- Location (FDA's records): Seongnam-Si, KR
- FDA decisions: 4 (2016–2025): 4 510(k) clearances
- Product codes: EKX (2), LQY (1), EBZ (1)
- 510(k) review time since 2016: median 274 days, against 274 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 1 (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
- Meta Biomed Co., Ltd.: 1 (https://510kreport.com/company/meta-biomed)
- J. Morita USA, Inc.: 1 (https://510kreport.com/company/j-morita-usa)
- S-Denti Co., Ltd.: 1 (https://510kreport.com/company/s-denti)
- Ultradent Products, Inc.: 1 (https://510kreport.com/company/ultradent-products)
- Dentall Co., Ltd.: 1 (https://510kreport.com/company/dentall)

## Firms that cite its devices most
- Schlumbohm GmbH & Co. KG: 1 (https://510kreport.com/company/schlumbohm)

## Its most-cited devices
- K153285: EMS-200 (2016), cited by 1

## Recent decisions
- K253461: Demi Pro (Oct 14, 2025)
- K210475: EQ-M (Sep 21, 2022)
- K210789: EQ-PEX (Oct 20, 2021)
- K153285: EMS-200 (Aug 12, 2016)

Source page: https://510kreport.com/company/meta-systems