Cultiv8 1, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cultiv8 1, LLC - FDA 510(k) Cleared Devices
Recent clearances: Genie MAX Large Bore Introducer Sheath
1
Total
1
Cleared
0
Denied
Cultiv8 1, LLC has 1 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Latest FDA clearance: Jan 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cultiv8 1, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cultiv8 1, LLC
1 devices