Cleared Traditional

K935625 - ALPHADENT LIGHT ACTIVATED ORTHODONTIC A...

K935625 is the FDA 510(k) clearance for ALPHADENT LIGHT ACTIVATED ORTHODONTIC A... by Wallace A. Erickson & Co.. It is a Class 2 Dental device (product code DYH) cleared through the Traditional 510(k) pathway after a 261-day FDA review.

K935625 · Wallace A. Erickson & Co. · Dental device
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Aug 1994
Decision
261d
Days
Class 2
Risk

K935625 is an FDA 510(k) clearance for the ALPHADENT LIGHT ACTIVATED ORTHODONTIC ADHESIVE BONDING SYSTEM WITH FLUORIDE. Classified as Adhesive, Bracket And Tooth Conditioner, Resin (product code DYH), Class II - Special Controls.

Submitted by Wallace A. Erickson & Co. (Chicago, US). The FDA issued a Cleared decision on August 10, 1994 after a review of 261 days - an extended review cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3750 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Dental review framework, consistent with the majority of Class II 510(k) submissions.

View all Wallace A. Erickson & Co. devices

Submission Details

510(k) Number K935625 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 22, 1993
Decision Date August 10, 1994
Days to Decision 261 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
134d slower than avg
Panel avg: 127d · This submission: 261d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DYH Adhesive, Bracket And Tooth Conditioner, Resin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3750
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 - DYH Adhesive, Bracket And Tooth Conditioner, Resin

All 115
Devices cleared under the same product code (DYH) and FDA review panel - the closest regulatory comparables to K935625.
THERMASET
K946255 · Ormco Corp. · Jan 1995
ALPHA BOND-RITE II(TM) OR BOND-RITE II(TM) 2-PASTE ADHEV
K942742 · Wallace A. Erickson & Co. · Aug 1994
ALPHA BOUND-RITE I NO-MIX ADHESIVE OR BOND-RITE I NO-MIX ADHESIVE
K942727 · Wallace A. Erickson & Co. · Aug 1994
SYSTEM 1
K940845 · Sybron Dental Specialties, Inc. · Mar 1994
ORMCO SYSTEM 1+ (TM)
K941015 · Ormco Corp. · Mar 1994
CRYSTALLINE L3 MULTI-USE HYBRID COMPOSITE
K935714 · Confi-Dental Products Co. · Jan 1994