HyperVit Vitrectomy Probe, 23 GA, HyperVit Vitrectomy Probe, 25+, HyperVit Vitrectomy Probe, 27+— 510(k) K170520

Substantially Equivalent

Alcon Research, Ltd.

FDA 510(k) clearance K170520 for HyperVit Vitrectomy Probe, 23 GA, HyperVit Vitrectomy Probe, 25+, HyperVit Vitrectomy Probe, 27+, Substantially Equivalent on 2017-03-22. Applicant: Alcon Research, Ltd..

Clearance details

Applicant: Alcon Research, Ltd.
Product code: Code MLZ
Advisory panel: Ophthalmic
Date received: 2017-02-22
Decision date: 2017-03-22
Decision: Substantially Equivalent
Clearance type: Special
Location: Lake Forest, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code MLZ

product code MLZ

Malfunction: 692
Total: 692

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.