CLEAR1-DAY HIOXIFILCON DAILY DISPOSABLE SOFT CONTACT LENS— 510(k) K080632

Substantially Equivalent

Clearlab SG Pte, Ltd.

FDA 510(k) clearance K080632 for CLEAR1-DAY HIOXIFILCON DAILY DISPOSABLE SOFT CONTACT LENS, Substantially Equivalent on 2008-10-15. Applicant: Clearlab SG Pte, Ltd..

Clearance details

Applicant: Clearlab SG Pte, Ltd.
Product code: Code MVN
Advisory panel: Ophthalmic
Date received: 2008-03-05
Decision date: 2008-10-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grand Junction, CO, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code MVN

product code MVN

Injury: 149
Total: 149

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.