Cleared Traditional

K050331 - ADHESIVE 1

K050331 is an FDA 510(k) clearance for ADHESIVE 1, manufactured by Southern Dental Industries, Inc.. The device is a Class 2 Dental device with product code KLE cleared through the Traditional 510(k) pathway after a 42-day FDA review.

K050331 · Southern Dental Industries, Inc. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2005
Decision
42d
Days
Class 2
Risk

K050331 is an FDA 510(k) clearance for the ADHESIVE 1. Classified as Agent, Tooth Bonding, Resin (product code KLE), Class II - Special Controls.

Submitted by Southern Dental Industries, Inc. (Bensenville, US). The FDA issued a Cleared decision on March 24, 2005 after a review of 42 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 Southern Dental Industries, Inc. devices

FDA 510(k) Submission Details - K050331

510(k) Number K050331 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 10, 2005
Decision Date March 24, 2005
Days to Decision 42 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
85d faster than avg
Panel avg: 127d · This submission: 42d
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 382
Devices cleared under the same product code (KLE) and FDA review panel - the closest regulatory comparables to K050331.
SEBOND PINK LIGHT 5G, SEBOND PINK DARK 5G, SEBOND SMART 5ML, SEBOND GRIP 3G, MODELS 644090, 644091, 640066, 644092
K051050 · Schutz-Dental GmbH · Jun 2005
IBOND NEXT GENERATION
K051006 · Heraeus Kulzer,GmbH · Jun 2005
ALL-IN-ONE
K050647 · Bisco, Inc. · Apr 2005
BOSWORTH BOND
K043170 · Harry J. Bosworth Co. · Feb 2005
PRIME & BOND NT DUAL CURE NANO-TECHNOLOGY UNIVERSAL DENTAL ADHESIVE SYSTEM
K050386 · Dentsply International · Feb 2005
HERMES BOND 2
K043043 · 3M Espe AG Dental Products · Jan 2005