DiaDent Group International

19 FDA 510(k) medical device clearances.

Top product codes for DiaDent Group International

KIF — Dental 6 devices
KLE — Dental 4 devices
EBF — Dental 3 devices
EBG — Dental 2 devices
EBZ — Dental 2 devices
ELW — Dental 1 device
EMA — Dental 1 device

Recent clearances by DiaDent Group International

K254112 — Dia-X Sil Bite ELW · 2026-03-19
K231552 — Dia-Cem EMA · 2023-07-28
K220804 — Dia-X Bond Universal KLE · 2022-06-15
K213401 — DIAPLUS Universal KLE · 2022-01-31
K210421 — Diafil & Diafil Capsule EBF · 2021-06-28
K210333 — DiaPaste KIF · 2021-03-25
K200174 — DIA-ROOT BIO MTA KIF · 2020-09-18
K200809 — D-LUX+ EBZ · 2020-08-07
K200175 — DIA-ROOT BIO Sealer KIF · 2020-06-25
K192392 — DiaPlus KLE · 2020-05-26
K190091 — Diapaste KIF · 2020-03-27
K192284 — DiaFil Flow EBF · 2020-03-25
K192510 — DIAFIL & DIAFIL Capsule EBF · 2020-03-20
K192022 — DiaTemp Flow EBG · 2020-02-13
K192158 — DiaTemp EBG · 2020-02-13
K192273 — DIAETCH Economic Package Type A, DIATECH Regular Package, DIAETCH Refill Package Type A, DIAETCH Intro Kit KLE · 2020-02-07
K182009 — Dia-Proseal KIF · 2019-09-26
K182625 — Diapex Plus KIF · 2019-06-03
K130163 — D-LUX EBZ · 2013-08-16

Data sourced from openFDA. This site is unofficial and independent of the FDA.