Genie MAX Large Bore Introducer Sheath— 510(k) K253652

Substantially Equivalent

Cultiv8 1, LLC

FDA 510(k) clearance K253652 for Genie MAX Large Bore Introducer Sheath, Substantially Equivalent on 2026-01-22. Applicant: Cultiv8 1, LLC.

Clearance details

Applicant: Cultiv8 1, LLC
Product code: Code DYB
Advisory panel: Cardiovascular
Date received: 2025-11-20
Decision date: 2026-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Plymouth, MN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DYB

product code DYB

Death: 808
Injury: 5,922
Malfunction: 16,516
Other: 5
Total: 23,251

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.