UNMIAX LAPAROSCOPIC INSTRUMENT— 510(k) K103508

Substantially Equivalent

Unimax Medical Systems, Inc.

FDA 510(k) clearance K103508 for UNMIAX LAPAROSCOPIC INSTRUMENT, Substantially Equivalent on 2011-12-20. Applicant: Unimax Medical Systems, Inc..

Clearance details

Applicant: Unimax Medical Systems, Inc.
Product code: Code GEI
Advisory panel: General, Plastic Surgery
Date received: 2010-11-29
Decision date: 2011-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taipei County, TW

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Adverse events under product code GEI

product code GEI

Death: 133
Injury: 7,585
Malfunction: 35,808
Other: 44
Total: 43,570

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.