# Rose K International, Ltd.

- Location (FDA's records): Hamilton, NZ
- FDA decisions: 2 (1995–2002): 2 510(k) clearances
- Product codes: HQD (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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 that cite its devices most
- Bausch & Lomb, Inc.: 1 (https://510kreport.com/company/bausch-lomb)
- Menicon Co, Ltd.: 1 (https://510kreport.com/company/menicon)
- Metro Optics of Austin, Inc.: 1 (https://510kreport.com/company/metro-optics-of-austin)

## Its most-cited devices
- K013646: Rose K Post Graft Lens (2002), cited by 2
- K945955: Rose K Lens (1995), cited by 1

## Recent decisions
- K013646: Rose K Post Graft Lens (May 30, 2002)
- K945955: Rose K Lens (Feb 7, 1995)

Source page: https://510kreport.com/company/rose-k-international