Medical Device Manufacturer · KR , Chungcheong Buk-Do

DiaDent Group International - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 2013

Recent clearances: DIAFIL, DIAFIL Bulk FLOW (Economic Package), Dia-X Sil Bite

Total

Cleared

Denied

DiaDent Group International has 21 FDA 510(k) cleared dental devices. Based in Chungcheong Buk-Do, KR.

Latest FDA clearance: Jun 2026. Active since 2013.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

DiaDent Group International is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - DiaDent Group International

21 devices

1-12 of 21

DIAFIL Bulk FLOW (Economic Package)

Diafil & Diafil Capsule

DiaDent Group International - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - DiaDent Group International

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