# Lorenz Biotech S.P.A.

- Location (FDA's records): North Attleboro, MA
- FDA decisions: 2 (2007–2008): 2 510(k) clearances
- Product codes: GXY (1), GZJ (1)
- Predicates its devices cite: 12 (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
- Empi: 2 (https://510kreport.com/company/empi)
- Apex Medical Corp.: 2 (https://510kreport.com/company/apex-medical)
- Andover Medical, Inc.: 1 (https://510kreport.com/company/andover-medical)
- Gemore Technology Co, Ltd.: 1 (https://510kreport.com/company/gemore-technology)
- Rehabilicare, Inc.: 1 (https://510kreport.com/company/rehabilicare)
- Sterne Equipment Co., Ltd.: 1 (https://510kreport.com/company/sterne-equipment)
- Chattanooga Group, Inc.: 1 (https://510kreport.com/company/chattanooga-group)
- Myotronics-Noromed, Inc.: 1 (https://510kreport.com/company/myotronics-noromed)

## Recent decisions
- K080902: Frems SSC Disposable Foam Electrodes, Model 800-000-057; Frems SSC Disposable Non-Woven Electrodes, Model 800-000-058 (Jun 13, 2008)
- K061828: Lorenz Biotech Aptiva, Version 2.13 (Aug 24, 2007)

Source page: https://510kreport.com/company/lorenz-biotech