Cleared Traditional

K100511 - COTEC DENTAL IMPLANT SYSTEM

K100511 is an FDA 510(k) clearance for COTEC DENTAL IMPLANT SYSTEM, manufactured by Cotec Implant Co., Ltd.. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 137-day FDA review.

K100511 · Cotec Implant Co., Ltd. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2010
Decision
137d
Days
Class 2
Risk

K100511 is an FDA 510(k) clearance for the COTEC DENTAL IMPLANT SYSTEM. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Cotec Implant Co., Ltd. (Santa Fe Springs, US). The FDA issued a Cleared decision on July 9, 2010 after a review of 137 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3640 - the FDA dental device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Dental review framework, consistent with the majority of Class II 510(k) submissions.

View all Cotec Implant Co., Ltd. devices

FDA 510(k) Submission Details - K100511

510(k) Number K100511 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 22, 2010
Decision Date July 09, 2010
Days to Decision 137 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
10d slower than avg
Panel avg: 127d · This submission: 137d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 922
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K100511.
HT III SA FIXTURE SYSTEM
K101096 · Hiossen, Inc. · Oct 2010
TAPERED SCREW-VENT T IMPLANT, TAPERED SCREW-VENT P IMPLANT
K101880 · Zimmer Dental, Inc. · Oct 2010
TAPERED SCREW-VENT T IMPLANT
K101977 · Zimmer Dental, Inc. · Sep 2010
MODIFICATION TO: HG III ULTRA WIDE SYSTEM
K093889 · Hiossen, Inc. · Apr 2010
BIOHORIZONS LASER-LOK 3.0 IMPLANT SYSTEM
K093321 · BioHorizons Implant Systems, Inc. · Apr 2010
SPI DENTAL IMPLANT, ELEMENT
K093615 · Thommen Medical AG · Mar 2010