Cleared Abbreviated

K041368 - DENTIUM CO.

K041368 is an FDA 510(k) clearance for DENTIUM CO., manufactured by Dentium Co., Ltd.. The device is a Class 2 Dental device with product code DZE cleared through the Abbreviated 510(k) pathway after a 66-day FDA review.

K041368 · Dentium Co., Ltd. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2004
Decision
66d
Days
Class 2
Risk

K041368 is an FDA 510(k) clearance for the DENTIUM CO., LTD. IMPLANTIUM. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Dentium Co., Ltd. (Dunwoody, US). The FDA issued a Cleared decision on July 29, 2004 after a review of 66 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3640 - the FDA dental device regulatory framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Dentium Co., Ltd. devices

FDA 510(k) Submission Details - K041368

510(k) Number K041368 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 24, 2004
Decision Date July 29, 2004
Days to Decision 66 days
Submission Type Abbreviated
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
61d faster than avg
Panel avg: 127d · This submission: 66d
Pathway characteristics
Standards-based clearance path.

DZE Device Classification - Class 2, Special Controls

Product Code DZE Implant, Endosseous, Root-form
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3640
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Dental devices follow this clearance model.

Regulatory Peers - DZE Implant, Endosseous, Root-form

All 792
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K041368.
NOBEL BIOCARE ENDOSSEOUS IMPLANTS
K041661 · Nobel Biocare Uas, Inc. · Aug 2004
NOBELDIRECT OD IMPLANT
K041876 · Nobel Biocare Uas, Inc. · Aug 2004
ASTRA TECH IMPLANTS - DENTAL SYSTEM
K041492 · Astra Tech, Inc. · Aug 2004
ACE CONNECT INTERNAL CONNECTION
K041759 · Ace Surgical Supply Co., Inc. · Jul 2004
MAXIMUS OS (OVERDENTURE SYSTEM)
K041938 · BioHorizons Implant Systems, Inc. · Jul 2004
STRAUMANN DENTAL IMPLANT SYSTEM
K033984 · Institut Straumann AG · Jun 2004