Elucid Bioimaging, Inc. is one of 16115 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Elucid Bioimaging, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Elucid FFR-IQ (B.1), Elucid PlaqueIQ, Elucid PlaqueIQ
6
Total
6
Cleared
0
Denied
Elucid Bioimaging, Inc. has 6 FDA 510(k) cleared medical devices. Based in Wenham, US.
Latest FDA clearance: Sep 2026. Active since 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Elucid Bioimaging, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Elucid Bioimaging, Inc.
6 devices
Cleared
Sep 29, 2026
Elucid FFR-IQ (B.1)
Cardiovascular
106d
Cleared
Sep 18, 2026
Elucid PlaqueIQ
Radiology
107d
Cleared
Sep 12, 2024
Elucid PlaqueIQ
Radiology
106d
Cleared
Jun 17, 2022
ElucidVivo A.3
Radiology
29d
Cleared
CT
Dec 21, 2018
vascuCAP
Radiology
51d
Cleared
May 24, 2017
vascuCAP
Radiology
203d