Vericom Co., Ltd.
Vericom Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2026.
Top product codes for Vericom Co., Ltd.
Recent clearances by Vericom Co., Ltd.
- K260805 — Dual Core
- K252285 — Well-Root PT
- K203672 — MAZIC Claro CAD and MAZIC Claro Press
- K193260 — U-Cem Premium & MAZIC Cem
- K170950 — Well-Root ST
- K163346 — MAZIC Duro
- K160377 — V-varnish Premium
- K152615 — Vonflex S
- K152518 — Vonflex S Putty
- K140966 — VONFLEX S BITE
- K103164 — VONFLEX HEAVY, VINFLEX LIGHT
- K103121 — ECO-S
- K091267 — VONFLEX PUTTY
- K090992 — WELL-PASTE
- K080265 — DENFIL ETCHANT-37
- K080266 — WELL-PEX
- K072069 — SPACER
- K060637 — DENFIL FLOW
- K043562 — BC PLUS
- K042124 — DENFIL
Data sourced from openFDA. This site is unofficial and independent of the FDA.