Cleared Traditional

K040857 - MODIFICATION TO ADPER PROMPT

K040857 is an FDA 510(k) clearance for MODIFICATION TO ADPER PROMPT, manufactured by 3M Espe AG Dental Products. The device is a Class 2 Dental device with product code KLE cleared through the Traditional 510(k) pathway after a 38-day FDA review.

K040857 · 3M Espe AG Dental Products · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 2004
Decision
38d
Days
Class 2
Risk

K040857 is an FDA 510(k) clearance for the MODIFICATION TO ADPER PROMPT. Classified as Agent, Tooth Bonding, Resin (product code KLE), Class II - Special Controls.

Submitted by 3M Espe AG Dental Products (Bavaria D-82228 Seefeld, DE). The FDA issued a Cleared decision on May 10, 2004 after a review of 38 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3200 - 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 3M Espe AG Dental Products devices

FDA 510(k) Submission Details - K040857

510(k) Number K040857 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 02, 2004
Decision Date May 10, 2004
Days to Decision 38 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
89d faster than avg
Panel avg: 127d · This submission: 38d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KLE Device Classification - Class 2, Special Controls

Product Code KLE Agent, Tooth Bonding, Resin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3200
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 - KLE Agent, Tooth Bonding, Resin

All 317
Devices cleared under the same product code (KLE) and FDA review panel - the closest regulatory comparables to K040857.
COMPOSITE/COMPOMER REPAIR KIT
K041960 · Dmg USA, Inc. · Aug 2004
G-BOND
K041471 · GC America, Inc. · Jun 2004
XENO NM LIGHT CURED DENTAL ADHESIVE
K041343 · Dentsply International · Jun 2004
HERMES BOND
K033974 · 3M Espe AG Dental Products · Feb 2004
CLEARFIL PROTECT BOND
K033938 · Kuraray Medical, Inc. · Jan 2004
EMBRACE WETBOND RESTORATION AND PFM REPAIR KIT
K032953 · Pulpdent Corporation · Dec 2003