Aibolit Technologies, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aibolit Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: AIBOLIT 3D+, AIBOLIT 3D+
2
Total
2
Cleared
0
Denied
Aibolit Technologies, LLC has 2 FDA 510(k) cleared medical devices. Based in Delray Beach, US.
Last cleared in 2023. Active since 2022. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Aibolit Technologies, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Howard Schrayer as regulatory consultant.
FDA 510(k) Regulatory Record - Aibolit Technologies, LLC
2 devices