MODIFICATION TO WARTNER WART REMOVAL SYSTEM— 510(k) K011708

Substantially Equivalent

Wartner Medical Products

FDA 510(k) clearance K011708 for MODIFICATION TO WARTNER WART REMOVAL SYSTEM, Substantially Equivalent on 2002-02-20. Applicant: Wartner Medical Products.

Clearance details

Applicant: Wartner Medical Products
Product code: Code GEH
Advisory panel: General, Plastic Surgery
Date received: 2001-06-04
Decision date: 2002-02-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brampton, Ontario, CA

Download summary PDF View on FDA.gov ↗

Adverse events under product code GEH

product code GEH

Death: 25
Injury: 351
Malfunction: 901
Total: 1,277

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.