LenSx Laser System (8065000944)— 510(k) K252682
Substantially EquivalentAlcon Laboratories, Inc.
FDA 510(k) clearance K252682 for LenSx Laser System (8065000944), Substantially Equivalent on 2025-09-24. Applicant: Alcon Laboratories, Inc..
Clearance details
- Applicant
- Alcon Laboratories, Inc.
- Product code
- Code OOE
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Fort Worth, TX, US
Adverse events under product code OOE
product code OOE- Injury
- 1,104
- Malfunction
- 864
- Total
- 1,968
Source: openFDA MAUDE database, through . 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.