Cleared Traditional

K921283 - ADHESIVE

K921283 is an FDA 510(k) clearance for ADHESIVE, manufactured by Jeneric/Pentron, Inc.. The device is a Class 2 Dental device with product code DYH cleared through the Traditional 510(k) pathway after a 281-day FDA review.

K921283 · Jeneric/Pentron, Inc. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 1992
Decision
281d
Days
Class 2
Risk

K921283 is an FDA 510(k) clearance for the ADHESIVE, BRACKET AND TOOTH CONDITIONER RESIN. Classified as Adhesive, Bracket And Tooth Conditioner, Resin (product code DYH), Class II - Special Controls.

Submitted by Jeneric/Pentron, Inc. (Wallingford, US). The FDA issued a Cleared decision on December 23, 1992 after a review of 281 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 Jeneric/Pentron, Inc. devices

FDA 510(k) Submission Details - K921283

510(k) Number K921283 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 17, 1992
Decision Date December 23, 1992
Days to Decision 281 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
154d slower than avg
Panel avg: 127d · This submission: 281d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DYH Device Classification - Class 2, Special Controls

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 126
Devices cleared under the same product code (DYH) and FDA review panel - the closest regulatory comparables to K921283.
CRYSTALLINE L3 MULTI-USE HYBRID COMPOSITE
K935714 · Confi-Dental Products Co. · Jan 1994
RESILIENCE ORTHODONTIC BRACKET ADHES W/BOND RESINS
K925359 · Confi-Dental Products Co. · Jul 1993
ALPHA-DENT ORTHODONTIC ADHES TWO-PASTE BOND SYST
K930614 · Wallace A. Erickson & Co. · Jun 1993
ALPHA-DENT ORTHODONTIC ADHESIVE WITH ONE STEP BOND
K921044 · Wallace A. Erickson & Co. · Nov 1992
CHALLENGE II - PASTE ADHESIVE
K923399 · Ormco Corp. · Oct 1992
THE BRACKET ASSEMBLY W/ SECURITY SYSTEM II
K921245 · Ormco Corp. · May 1992