Cleared Traditional

K031811 - PIT & FISSURE SEALANT WITH FLUORIDE

K031811 is the FDA 510(k) clearance for PIT & FISSURE SEALANT WITH FLUORIDE by Harry J. Bosworth Co.. It is a Class 2 Dental device (product code EBC) cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K031811 · Harry J. Bosworth Co. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 2003
Decision
84d
Days
Class 2
Risk

K031811 is an FDA 510(k) clearance for the PIT & FISSURE SEALANT WITH FLUORIDE. Classified as Sealant, Pit And Fissure, And Conditioner (product code EBC), Class II - Special Controls.

Submitted by Harry J. Bosworth Co. (Skokie, US). The FDA issued a Cleared decision on September 4, 2003 after a review of 84 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3765 - 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 Harry J. Bosworth Co. devices

Submission Details

510(k) Number K031811 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 12, 2003
Decision Date September 04, 2003
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.

Device Classification

Product Code EBC Sealant, Pit And Fissure, And Conditioner
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3765
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 - EBC Sealant, Pit And Fissure, And Conditioner

All 58
Devices cleared under the same product code (EBC) and FDA review panel - the closest regulatory comparables to K031811.
ADMIRA PROTECT/ADMIRA PROTECT SINGLE DOSE
K061823 · Voco GmbH · Jul 2006
BOSWORTH SEAL
K051224 · Harry J. Bosworth Co. · Jul 2005
AEGIS PIT & FISSURE SEALANT WITH ACP
K033751 · Harry J. Bosworth Co. · Feb 2004
ADMIRA SEAL
K021842 · Voco GmbH · Jul 2002
ADMIRA PROTECT
K021844 · Voco GmbH · Jul 2002
REVOTEK LC
K012542 · GC America, Inc. · Oct 2001