Swift Sync, Inc. is one of 16326 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Swift Sync, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Sync AV II Temporary Pacing Catheter
1
Total
1
Cleared
0
Denied
Swift Sync, Inc. has 1 FDA 510(k) cleared medical devices. Based in Miami Shores, US.
Latest FDA clearance: Jul 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Swift Sync, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by RQM+ as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Swift Sync, Inc.
1 devices