Soundbite Medical Solutions, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Soundbite Medical Solutions, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SoundBite® Crossing System XS Peripheral, SoundBite Crossing System - Peripheral (14P)
2
Total
2
Cleared
0
Denied
Soundbite Medical Solutions, Inc. has 2 FDA 510(k) cleared medical devices. Based in Montreal, CA.
Last cleared in 2023. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Soundbite Medical Solutions, 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 - Soundbite Medical Solutions, Inc.
2 devices