Cleared Traditional

K103027 - ELECTROTORQUE TLC

K103027 is the FDA 510(k) clearance for ELECTROTORQUE TLC by Kaltenbach & Voigt GmbH. It is a Class 1 Dental device (product code EBW) cleared through the Traditional 510(k) pathway after a 310-day FDA review.

K103027 · Kaltenbach & Voigt GmbH · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2011
Decision
310d
Days
Class 1
Risk

K103027 is an FDA 510(k) clearance for the ELECTROTORQUE TLC. Classified as Controller, Foot, Handpiece And Cord (product code EBW), Class I - General Controls.

Submitted by Kaltenbach & Voigt GmbH (Orange, US). The FDA issued a Cleared decision on August 19, 2011 after a review of 310 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.4200 - 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. Elevated predicate reliance profile. 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 Kaltenbach & Voigt GmbH devices

Submission Details

510(k) Number K103027 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 13, 2010
Decision Date August 19, 2011
Days to Decision 310 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
183d slower than avg
Panel avg: 127d · This submission: 310d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code EBW Controller, Foot, Handpiece And Cord
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.4200
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - EBW Controller, Foot, Handpiece And Cord

All 25
Devices cleared under the same product code (EBW) and FDA review panel - the closest regulatory comparables to K103027.
Surgic Pro, Surgic Pro+
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K992648 · J. Morita USA, Inc. · Jan 2000