DiaPaste— 510(k) K210333

Substantially Equivalent

DiaDent Group International

FDA 510(k) clearance K210333 for DiaPaste, Substantially Equivalent on 2021-03-25. Applicant: DiaDent Group International. Device class: 2.

Clearance details

Applicant: DiaDent Group International
Product code: Product code KIF
Device class: Class 2
Regulation: 21 CFR 872.3820
Advisory panel: Dental
Date received: 2021-02-05
Decision date: 2021-03-25
Decision: Substantially Equivalent
Clearance type: Special
Location: Cheongju-Si, KR

Download summary PDF View on FDA.gov ↗

Recent devices under product code KIF

K262050 — Vioseal X2026-09-11
K253909 — NeoPEX Pre-Mixed Obturation Paste2026-09-04
K261514 — Calcium Hydroxide Temporary Filling Material (KP-Cal)2026-08-25
K261415 — Injectable Root Canal Sealer (KP-Root SP)2026-06-29
K253167 — Any-Paste2026-01-12

More clearances from DiaDent Group International

K254142 — Dia-X Sil Heavy Body2026-09-16
K254152 — Dia-X Sil Light Body2026-09-16
K261166 — DIA-CEM2026-07-09
K261093 — DIAFIL2026-06-02
K261071 — DIAFIL Bulk FLOW (3 models)2026-05-19

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