Cleared Traditional

K010994 - TAKE ONE BITE MODIFIED

K010994 is an FDA 510(k) clearance for TAKE ONE BITE MODIFIED, manufactured by Kerr Corp.. The device is a Class 2 Dental device with product code ELW cleared through the Traditional 510(k) pathway after a 20-day FDA review.

K010994 · Kerr Corp. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 2001
Decision
20d
Days
Class 2
Risk

K010994 is an FDA 510(k) clearance for the TAKE ONE BITE MODIFIED. Classified as Material, Impression (product code ELW), Class II - Special Controls.

Submitted by Kerr Corp. (Orange, US). The FDA issued a Cleared decision on April 23, 2001 after a review of 20 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3660 - 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.

View all Kerr Corp. devices

FDA 510(k) Submission Details - K010994

510(k) Number K010994 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 03, 2001
Decision Date April 23, 2001
Days to Decision 20 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
107d faster than avg
Panel avg: 127d · This submission: 20d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

ELW Device Classification - Class 2, Special Controls

Product Code ELW Material, Impression
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3660
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 - ELW Material, Impression

All 265
Devices cleared under the same product code (ELW) and FDA review panel - the closest regulatory comparables to K010994.
EXTRUDE MODIFIED
K012405 · Sybron Dental Specialties, Inc. · Sep 2001
CAVEX STABISIL
K011452 · Cavex Holland BV · Jul 2001
CAVEX COLORCHANGE
K011419 · Cavex Holland BV · Jul 2001
TAKE 1
K003808 · Sybron Dental Specialties, Inc. · Mar 2001
PERMLASTIC 3
K003650 · Sybron Dental Specialties, Inc. · Feb 2001
FLEXTIME MAGNUM 360
K003930 · Heraeus Kulzer, Inc. · Feb 2001