# Overture Resurfacing, Inc.

- Location (FDA's records): New York, NY
- FDA decisions: 2 (2023–2023): 2 510(k) clearances
- Product codes: KRR (1), HSX (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (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
- Arthrosurface, Inc.: 2 (https://510kreport.com/company/arthrosurface)

## Firms that cite its devices most
- Overture Orthopaedics: 1 (https://510kreport.com/company/overture-orthopaedics)

## Its most-cited devices
- K221292: Uni Knee Resurfacing System (2023), cited by 1

## Recent decisions
- K231253: Overture Orthopaedics Patellofemoral System (Jul 7, 2023)
- K221292: Uni Knee Resurfacing System (Mar 10, 2023)

Source page: https://510kreport.com/company/overture-resurfacing