Graphy, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Graphy, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TERA HARZ Hard Denture (THD-C-500), TERA HARZ CLEAR, TERA HARZ II
6
Total
6
Cleared
0
Denied
Graphy, Inc. has 6 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: Nov 2025. Active since 2021. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Graphy, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Third Party Review Group, LLC and Plusglobal.
FDA 510(k) Regulatory Record - Graphy, Inc.
6 devices