# Feeltech Co., Ltd.

- Location (FDA's records): Gunsan-Si, KR
- FDA decisions: 4 (2018–2025): 4 510(k) clearances
- Product codes: NEW (3), QNQ (1)
- 510(k) review time since 2016: median 273 days, against 146 for FDA's reviews in the same codes and years (0 of 3 faster)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 4 (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
- Demetech Corp.: 1 (https://510kreport.com/company/demetech)
- ETHICON, Inc.: 1 (https://510kreport.com/company/ethicon)
- Surgical Specialties Corp. Dba Angiotech: 1 (https://510kreport.com/company/surgical-specialties-dba-angiotech)
- Jiangsu Caina Medical Co.,Ltd: 1 (https://510kreport.com/company/jiangsu-caina-medical)

## Firms that cite its devices most
- Hyundae Meditech Co., Ltd.: 1 (https://510kreport.com/company/hyundae-meditech)
- Medexel Co.,Ltd: 1 (https://510kreport.com/company/medexel)
- Pdo Max, Inc.: 1 (https://510kreport.com/company/pdo-max)

## Its most-cited devices
- K172602: Miracu (2018), cited by 3
- K213010: FEELject LDV (Low dead volume) syringe (2023), cited by 1

## Recent decisions
- K251414: Miracu™ Polydioxanone (PDO) Suture and Needle (MONO) (Oct 20, 2025)
- K250107: V-soft Line™ Barbed Surgical Suture (Various) (Oct 15, 2025)
- K213010: FEELject LDV (Low dead volume) syringe (May 31, 2023)
- K172602: Miracu (Nov 14, 2018)

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