VISTAKON (HEFILCON C) CONTACT LENSES— 510(k) K010218

Substantially Equivalent

Vistakon

FDA 510(k) clearance K010218 for VISTAKON (HEFILCON C) CONTACT LENSES, Substantially Equivalent on 2001-03-16. Applicant: Vistakon.

Clearance details

Applicant: Vistakon
Product code: Code LPL
Advisory panel: Ophthalmic
Date received: 2001-01-24
Decision date: 2001-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

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Adverse events under product code LPL

product code LPL

Injury: 988
Other: 4
Total: 992

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.