# The O R Company Pty, Ltd.

- Location (FDA's records): Carrum Downs, AU
- FDA decisions: 2 (2022–2022): 2 510(k) clearances
- Product codes: LKF (2)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (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
- Panpac Medical Corporation: 1 (https://510kreport.com/company/panpac-medical)
- Conmed Corporation: 1 (https://510kreport.com/company/conmed)

## Recent decisions
- K220202: Uterine ElevatOR PRO with OccludOR Balloon (Mar 31, 2022)
- K212505: DUMI ManipulatOR (Jan 10, 2022)

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