IRIDEX OTOPROBE LONG AND SHORT ANGLES, P/N 14310-1 AND 14320-1— 510(k) K060905

Substantially Equivalent

Iridex Corp

FDA 510(k) clearance K060905 for IRIDEX OTOPROBE LONG AND SHORT ANGLES, P/N 14310-1 AND 14320-1, Substantially Equivalent on 2006-05-31. Applicant: Iridex Corp.

Clearance details

Applicant: Iridex Corp
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 2006-04-03
Decision date: 2006-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mountain View, CA, US

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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.