Glytec, LLC is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Glytec, LLC - FDA 510(k) Cleared Devices
Recent clearances: Glucommander, Glucommander, Glucommander
4
Total
4
Cleared
0
Denied
Glytec, LLC has 4 FDA 510(k) cleared medical devices. Based in Greenville, US.
Latest FDA clearance: Oct 2026. Active since 2012. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Glytec, LLC Filter by specialty or product code using the sidebar.
2 submissions have an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.
FDA 510(k) Regulatory Record - Glytec, LLC
4 devices