# Limacorporate

- Location (FDA's records): Villanova Di San Daniele Del Friuli, IT
- FDA decisions: 4 (2019–2025): 4 510(k) clearances
- Product codes: JWH (2), LZO (1), KWS (1)
- 510(k) review time since 2016: median 121 days, against 126 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 10 (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
- Lima Corporate S.P.A.: 8 (https://510kreport.com/company/lima-corporate)
- Total Joint Othopedics, Inc.: 1 (https://510kreport.com/company/total-joint-othopedics)
- Biomet UK, Ltd.: 1 (https://510kreport.com/company/biomet-uk)

## Firms that cite its devices most
- Lima Corporate S.P.A.: 1 (https://510kreport.com/company/lima-corporate)

## Its most-cited devices
- K190911: Physica KR Liner and SMR Reverse Humeral Liner (2019), cited by 1

## Recent decisions
- K243809: Biolox® Delta Revision heads (Mar 4, 2025)
- K213785: SMR TT Hybrid Glenoid, SMR 3-Pegs Cemented Glenoid (May 13, 2022)
- K211938: Physica LMC Knee System (Jul 13, 2021)
- K190911: Physica KR Liner and SMR Reverse Humeral Liner (Nov 26, 2019)

Source page: https://510kreport.com/company/limacorporate