# Piezosurgery S.R.L.

- Location (FDA's records): Rome, IT
- FDA decisions: 4 (2005–2009): 4 510(k) clearances
- Product codes: DZI (2), JDX (1), ELC (1)
- Predicates its devices cite: 6 (2 its own); citations of its devices by later devices: 10 (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
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Linvatec Corp.: 1 (https://510kreport.com/company/linvatec)
- Electro Medical Systems SA: 1 (https://510kreport.com/company/electro-medical-systems)
- Nouvag AG: 1 (https://510kreport.com/company/nouvag)

## Firms that cite its devices most
- Satelec: 2 (https://510kreport.com/company/satelec)
- Mectron S.P.A.: 2 (https://510kreport.com/company/mectron)
- Silfradent S.R.L.: 1 (https://510kreport.com/company/silfradent)
- Dong IL Technology, Ltd.: 1 (https://510kreport.com/company/dong-il-technology)
- Guilin Woodpecker Medical Instrument Co., Ltd.: 1 (https://510kreport.com/company/guilin-woodpecker-medical-instrument)
- E.M.S Electro Medical Systems S.A: 1 (https://510kreport.com/company/ems-electro-medical-systems-s-a)

## Its most-cited devices
- K043408: Piezosurgery Device (2005), cited by 5
- K083284: Piezosurgery Medical (2009), cited by 2
- K091227: Piezosurgery 3; Osstem Piezo (2009), cited by 2
- K052518: Piezosurgery (2005), cited by 1

## Recent decisions
- K091227: Piezosurgery 3; Osstem Piezo (Dec 29, 2009)
- K083284: Piezosurgery Medical (Apr 8, 2009)
- K052518: Piezosurgery (Nov 16, 2005)
- K043408: Piezosurgery Device (Jun 8, 2005)

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