PIEZOSURGERY— 510(k) K052518

Substantially Equivalent

Piezosurgery S.R.L.

FDA 510(k) clearance K052518 for PIEZOSURGERY, Substantially Equivalent on 2005-11-16. Applicant: Piezosurgery S.R.L..

Clearance details

Applicant: Piezosurgery S.R.L.
Product code: Code ELC
Advisory panel: Dental
Date received: 2005-09-14
Decision date: 2005-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rome, IT

Download summary PDF View on FDA.gov ↗

Adverse events under product code ELC

product code ELC

Malfunction: 1,255
Total: 1,255

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.