# Arcuro Medical, Ltd.

- Location (FDA's records): Misgav, IL
- FDA decisions: 3 (2018–2025): 3 510(k) clearances
- Product codes: GAT (2), MBI (1)
- 510(k) review time since 2016: median 133 days, against 95 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 2 (2 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
- T.A.G. Medical Products Corporation, Ltd.: 1 (https://510kreport.com/company/tag-medical-products)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)

## Its most-cited devices
- K180191: SuperBall Meniscal Repair System (2018), cited by 1
- K223500: SuperBall Meniscal Repair System (2023), cited by 1

## Recent decisions
- K244015: SuperBall-RC™ (Feb 19, 2025)
- K223500: SuperBall Meniscal Repair System (Aug 10, 2023)
- K180191: SuperBall Meniscal Repair System (Jun 5, 2018)

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