Cleared Traditional

K070723 - FUTURABOND DC/SINGLE DOSE

K070723 is an FDA 510(k) clearance for FUTURABOND DC/SINGLE DOSE, manufactured by Voco GmbH. The device is a Class 2 Dental device with product code KLE cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K070723 · Voco GmbH · Dental device
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Jun 2007
Decision
84d
Days
Class 2
Risk

K070723 is an FDA 510(k) clearance for the FUTURABOND DC/SINGLE DOSE. Classified as Agent, Tooth Bonding, Resin (product code KLE), Class II - Special Controls.

Submitted by Voco GmbH (Cuxhaven, DE). The FDA issued a Cleared decision on June 7, 2007 after a review of 84 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 Voco GmbH devices

FDA 510(k) Submission Details - K070723

510(k) Number K070723 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 15, 2007
Decision Date June 07, 2007
Days to Decision 84 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
43d faster than avg
Panel avg: 127d · This submission: 84d
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 372
Devices cleared under the same product code (KLE) and FDA review panel - the closest regulatory comparables to K070723.
UNO
K071131 · 3M Espe AG Dental Products · Jul 2007
HERMES BOND 3
K071260 · 3M Espe AG Dental Products · Jul 2007
FL BOND II
K071452 · Shofu Dental Corp. · Jul 2007
ADHESE ONE
K070646 · Ivoclar Vivadent, Inc. · May 2007
ASCENT UNIVERSAL ADHESIVE, MODEL 006-00028
K070413 · CAO Group, Inc. · Apr 2007
TOKUYAMA BOND FORCE
K070215 · Tokuyama Dental Corporation · Mar 2007