AESCULAP OPTILENE NONABSORBABLE SUTURE— 510(k) K133890

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K133890 for AESCULAP OPTILENE NONABSORBABLE SUTURE, Substantially Equivalent on 2014-07-15. Applicant: Aesculap, Inc..

Clearance details

Applicant: Aesculap, Inc.
Product code: Code GAW
Advisory panel: General, Plastic Surgery
Date received: 2013-12-20
Decision date: 2014-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Center Valley, PA, US

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Adverse events under product code GAW

product code GAW

Death: 66
Injury: 1,616
Malfunction: 10,428
Total: 12,110

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.