# Rootloc Co., Ltd.

- Location (FDA's records): Geumcheon-Gu, KR
- FDA decisions: 2 (2018–2018): 2 510(k) clearances
- Product codes: JWH (2)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 3 (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
- The Progressive Orthopaedic Company, LLC: 2 (https://510kreport.com/company/progressive-orthopaedic)
- United Orthopedic Corporation: 1 (https://510kreport.com/company/united-orthopedic)
- Corentec Co., Ltd.: 1 (https://510kreport.com/company/corentec)
- Novosource, Inc.: 1 (https://510kreport.com/company/novosource)

## Firms that cite its devices most
- L and K Biomed Corporation Limited: 1 (https://510kreport.com/company/l-and-k-biomed)
- Tjc Life Co., Ltd.: 1 (https://510kreport.com/company/tjc-life)

## Its most-cited devices
- K170753: Acculoc Total Knee System (2018), cited by 3

## Recent decisions
- K182370: Acculoc Total Knee System (Sep 27, 2018)
- K170753: Acculoc Total Knee System (Mar 23, 2018)

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