Cleared Traditional

K012944 - POWER DRIVE

K012944 is an FDA 510(k) clearance for POWER DRIVE, manufactured by Mediteam AB. The device is a Class 1 Dental device with product code EKX cleared through the Traditional 510(k) pathway after a 77-day FDA review.

K012944 · Mediteam AB · Dental device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Nov 2001
Decision
77d
Days
Class 1
Risk

K012944 is an FDA 510(k) clearance for the POWER DRIVE. Classified as Handpiece, Direct Drive, Ac-powered (product code EKX), Class I - General Controls.

Submitted by Mediteam AB (Savedalen, SE). The FDA issued a Cleared decision on November 20, 2001 after a review of 77 days - a notably fast clearance cycle.

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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

FDA 510(k) Submission Details - K012944

510(k) Number K012944 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 04, 2001
Decision Date November 20, 2001
Days to Decision 77 days
Submission Type Traditional
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
51d faster than avg
Panel avg: 128d · This submission: 77d
Pathway characteristics
Predicate-based equivalence.

EKX Device Classification - Class 1, General Controls

Product Code EKX Handpiece, Direct Drive, Ac-powered
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 - EKX Handpiece, Direct Drive, Ac-powered

All 89
Devices cleared under the same product code (EKX) and FDA review panel - the closest regulatory comparables to K012944.
DENTAPORT ZX
K031204 · J. Morita USA, Inc. · Aug 2003
APEX ELECTRIC HANDPIECE SYSTEM
K031540 · Lares Research, Inc. · Jun 2003
ASEPTICO VCT VERSATILE COMMAND TECHNOLOGY MODEL AEU-925
K030163 · Aseptico, Inc. · Mar 2003
OSSTELL RESONANCE FREQUENCY ANALYZER
K003714 · Integration Diagnostics, Ltd. · Aug 2001
ENDOSTEPPER 1
K993188 · Phytron- Elektronik GmbH · Sep 1999
QUANTEC-E ENDO SYSTEM
K990739 · Sybron Dental Specialties, Inc. · May 1999
K012944 · POWER DRIVE
Download PDF FDA Summary Mediteam AB