# Medexel Co.,Ltd

- Location (FDA's records): Anseong-Si, KR
- FDA decisions: 3 (2016–2024): 3 510(k) clearances
- Product codes: FMI (2), QNQ (1)
- 510(k) review time since 2016: median 266 days, against 182 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 2 (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
- Feel Tech: 1 (https://510kreport.com/company/feel-tech)
- Feeltech Co., Ltd.: 1 (https://510kreport.com/company/feeltech)

## Firms that cite its devices most
- CMT Health PTE., Ltd.: 1 (https://510kreport.com/company/cmt-health)
- W. L. Med Co., Ltd.: 1 (https://510kreport.com/company/w-l-med)

## Its most-cited devices
- K231856: TopFine® LDS (Low Dead Space) Syringe (2 models (TS-LDS2334, TS-LDS2534)) (2024), cited by 1
- K172095: Autokeeper (2018), cited by 1

## Recent decisions
- K231856: TopFine® LDS (Low Dead Space) Syringe (2 models (TS-LDS2334, TS-LDS2534)) (Mar 15, 2024)
- K172095: Autokeeper (Jul 24, 2018)
- K152410: Top Fine Pen Needle (Feb 2, 2016)

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