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# FDA Clears Vasorum Vascular Closure Device
- URL: https://www.fdaweb.com/fda-clears-vasorum-vascular-closure-device/
- Published: 2025-03-27T12:00:00.000Z
- Updated: 2026-09-14T14:56:27.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5158910

FDA has cleared a Vasorum 510(k) for the Celt ACD Plus vascular closure device, its next-generation device that it says provides physicians with a visual indicator for precise placement and closure, particularly in cases where ultrasound imaging is not available. The device is available in 5F, 6F, and 7F sizes.

The small-bore closure device is designed for rapid arterial puncture closure following percutaneous catheter-based vascular procedures, the company says. “Its novel mechanism of action reduces major vascular closure complications such as bleeding, hematomas, and pseudoaneurysms,” it says. “Clinical data has demonstrated significant reductions in time to hemostasis, ambulation, and discharge, leading to improved efficiency and cost savings in post-anesthesia care.”