Hdi, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Hdi, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DENU Light Body(Regular, Fast), DENU Heavy Body(Regular, Fast), DENU Putty Set(Regular, Fast), DENU Composite Resin, DENU Flow Resin
2
Total
2
Cleared
0
Denied
Hdi, Inc. has 2 FDA 510(k) cleared medical devices. Based in Seongnam-Si, KR.
Last cleared in 2022. Active since 2022. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Hdi, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hdi, Inc.
2 devices