DiaDent Group International
DiaDent Group International holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2026.
Top product codes for DiaDent Group International
Recent clearances by DiaDent Group International
- K261166 — DIA-CEM
- K261093 — DIAFIL
- K261071 — DIAFIL Bulk FLOW (3 models)
- K254112 — Dia-X Sil Bite
- K231552 — Dia-Cem
- K220804 — Dia-X Bond Universal
- K213401 — DIAPLUS Universal
- K210421 — Diafil & Diafil Capsule
- K210333 — DiaPaste
- K200174 — DIA-ROOT BIO MTA
- K200809 — D-LUX+
- K200175 — DIA-ROOT BIO Sealer
- K192392 — DiaPlus
- K190091 — Diapaste
- K192284 — DiaFil Flow
- K192510 — DIAFIL & DIAFIL Capsule
- K192022 — DiaTemp Flow
- K192158 — DiaTemp
- K192273 — DIAETCH Economic Package Type A, DIATECH Regular Package, DIAETCH Refill Package Type A, DIAETCH Intro Kit
- K182009 — Dia-Proseal
- K182625 — Diapex Plus
- K130163 — D-LUX
Data sourced from openFDA. This site is unofficial and independent of the FDA.