INCISOR I PULSED ND:YAG LASER SYSTEM— 510(k) K922901

Substantially Equivalent

Buckman Co., Inc.

FDA 510(k) clearance K922901 for INCISOR I PULSED ND:YAG LASER SYSTEM, Substantially Equivalent on 1992-11-20. Applicant: Buckman Co., Inc..

Clearance details

Applicant: Buckman Co., Inc.
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 1992-06-16
Decision date: 1992-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Concord, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GEX

product code GEX

Death: 33
Injury: 3,045
Malfunction: 12,903
Other: 25
Total: 16,006

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.