Su-Ko Technologies, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Su-Ko Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: SER Pen Carain MicroSystem (MP1209SP), SER Pen Carain MicroSystem (MP1209SP)
2
Total
2
Cleared
0
Denied
Su-Ko Technologies, LLC has 2 FDA 510(k) cleared medical devices. Based in Houston, US.
Latest FDA clearance: Oct 2025. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Su-Ko Technologies, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Contract In-House Counsel and Consultants, and Contract In-House Counsel and Consultants, LLC D/B/A FDA Att.
FDA 510(k) Regulatory Record - Su-Ko Technologies, LLC
2 devices