Dyne Medical Group, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Dyne Medical Group, Inc. - FDA 510(k) Cleared Devices
Recent clearances: URUS System (DMG-SU100/URUS)
2
Total
2
Cleared
0
Denied
Dyne Medical Group, Inc. has 2 FDA 510(k) cleared medical devices. Based in Gyeonggi-Do, KR.
Latest FDA clearance: Jun 2026. Active since 2024. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Dyne Medical Group, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Gms Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Dyne Medical Group, Inc.
2 devices