Dentium Co., Ltd.

22 FDA 510(k) medical device clearances.

Top product codes for Dentium Co., Ltd.

NHA — Dental 12 devices
DZE — Dental 9 devices
EBW — Dental 1 device

Recent clearances by Dentium Co., Ltd.

K213599 — SuperLine DZE · 2022-02-23
K193341 — iCTmotor (WL-1) EBW · 2020-09-04
K192436 — Healing Abutments and Cover Screws NHA · 2020-01-23
K191634 — Scan Abutments and Comfort Caps NHA · 2019-11-04
K172640 — Dentium Implantium & SuperLine Prosthetics NHA · 2018-05-14
K171622 — Dentium Ti-Base NHA · 2018-01-11
K171126 — Implantium II DZE · 2017-09-07
K170384 — Dentium NR Line CAD/CAM Abutments NHA · 2017-08-17
K160965 — SuperLine DZE · 2017-01-13
K161713 — Dentium CAD/CAM Abutments NHA · 2016-12-16
K160828 — Dentium Implantium & SuperLine Prosthetics NHA · 2016-09-15
K160483 — Burn-out Cylinder and Angled Screw Abutments NHA · 2016-08-05
K153268 — NR Line Implant System DZE · 2016-07-20
K141457 — DENTIUM IMPLANTIUM AND SUPERLINE ABUTMENTS NHA · 2014-11-12
K112045 — SIMPLELINE II ABUTMENT SYSTEM NHA · 2012-01-26
K111162 — SLIM ONEBODY SYSTEM DZE · 2012-01-13
K102308 — SIMPLELINE II MODEL SOFX483408R, SOFX483410R TOTAL 44 MODELS DZE · 2010-11-22
K070228 — IMPLANTIUM PROSTHETICS NHA · 2007-11-20
K052957 — IMPLANTIUM PROSTHETICS NHA · 2006-07-27
K060500 — SPEEDY ORTHODONTIC SCREW DZE · 2006-06-16
K060501 — IMPLANTIUM II DZE · 2006-06-16
K041368 — DENTIUM CO., LTD. IMPLANTIUM DZE · 2004-07-29

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