# R&R Medical Corporation, Ltd.

- Location (FDA's records): New Taipei City, TW
- FDA decisions: 4 (2005–2023): 4 510(k) clearances
- Names in FDA's records: R&R Medical Corporation, Ltd. (2); R&R Medical, Inc. (2)
- Product codes: KTT (2), FXX (1), NUC (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 8 (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
- Wuhan Dymex Healthcare Co., Ltd.: 1 (https://510kreport.com/company/wuhan-dymex-healthcare)
- Thai Nippon Rubber Industry Co., Ltd.: 1 (https://510kreport.com/company/thai-nippon-rubber-industry)
- Applied Osteo Systems, Inc.: 1 (https://510kreport.com/company/applied-osteo-systems)
- Electro-Biology, Inc.: 1 (https://510kreport.com/company/electro-biology)
- Ebi, L.P.: 1 (https://510kreport.com/company/ebi)

## Firms that cite its devices most
- Wrightmedicaltechnologyinc: 3 (https://510kreport.com/company/wrightmedicaltechnologyinc)
- Dne, LLC: 2 (https://510kreport.com/company/dne)
- Wright Medical Corp.: 2 (https://510kreport.com/company/wright-medical)
- Vilex, LLC: 1 (https://510kreport.com/company/vilex)

## Its most-cited devices
- K052005: R&R External Fixation System (2005), cited by 6
- K043174: Stealth Fusion System, Model RR 1000 (2005), cited by 2

## Recent decisions
- K220226: X-Y Lubricating Jelly (Mar 28, 2023)
- K214035: LAITEST Medical Face Mask (Sep 13, 2022)
- K052005: R&R External Fixation System (Sep 6, 2005)
- K043174: Stealth Fusion System, Model RR 1000 (Feb 7, 2005)

Source page: https://510kreport.com/company/r-r-medical