Dentium Co., Ltd.
Dentium Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2022.
Top product codes for Dentium Co., Ltd.
Recent clearances by Dentium Co., Ltd.
- K213599 — SuperLine
- K193341 — iCTmotor (WL-1)
- K192436 — Healing Abutments and Cover Screws
- K191634 — Scan Abutments and Comfort Caps
- K172640 — Dentium Implantium & SuperLine Prosthetics
- K171622 — Dentium Ti-Base
- K171126 — Implantium II
- K170384 — Dentium NR Line CAD/CAM Abutments
- K160965 — SuperLine
- K161713 — Dentium CAD/CAM Abutments
- K160828 — Dentium Implantium & SuperLine Prosthetics
- K160483 — Burn-out Cylinder and Angled Screw Abutments
- K153268 — NR Line Implant System
- K141457 — DENTIUM IMPLANTIUM AND SUPERLINE ABUTMENTS
- K112045 — SIMPLELINE II ABUTMENT SYSTEM
- K111162 — SLIM ONEBODY SYSTEM
- K102308 — SIMPLELINE II MODEL SOFX483408R, SOFX483410R TOTAL 44 MODELS
- K070228 — IMPLANTIUM PROSTHETICS
- K052957 — IMPLANTIUM PROSTHETICS
- K060500 — SPEEDY ORTHODONTIC SCREW
- K060501 — IMPLANTIUM II
- K041368 — DENTIUM CO., LTD. IMPLANTIUM
Data sourced from openFDA. This site is unofficial and independent of the FDA.