LENSX LASER SYSTEM— 510(k) K123120

Substantially Equivalent

Alcon Lensx, Inc.

FDA 510(k) clearance K123120 for LENSX LASER SYSTEM, Substantially Equivalent on 2012-12-12. Applicant: Alcon Lensx, Inc..

Clearance details

Applicant: Alcon Lensx, Inc.
Product code: Code OOE
Advisory panel: Ophthalmic
Date received: 2012-10-03
Decision date: 2012-12-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Laguna Beach, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code OOE

product code OOE

Injury: 1,104
Malfunction: 864
Total: 1,968

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.