Synergen Technology Labs, LLC is one of 5575 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Synergen Technology Labs, LLC - FDA 510(k) Cleared Devices
Recent clearances: ScioCardio ECG Transmitter
2
Total
2
Cleared
0
Denied
Synergen Technology Labs, LLC has 2 FDA 510(k) cleared medical devices. Based in Dallas, US.
Latest FDA clearance: Jul 2026. Active since 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Synergen Technology Labs, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kamm & Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Synergen Technology Labs, LLC
2 devices