Cleared Traditional

K111668 - CAVIOS CAVITY LINER

K111668 is an FDA 510(k) clearance for CAVIOS CAVITY LINER, manufactured by Neodental Chemical Products Co., Ltd.. The device is a Class 2 Dental device with product code EJK cleared through the Traditional 510(k) pathway after a 66-day FDA review.

K111668 · Neodental Chemical Products Co., Ltd. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2011
Decision
66d
Days
Class 2
Risk

K111668 is an FDA 510(k) clearance for the CAVIOS CAVITY LINER. Classified as Liner, Cavity, Calcium Hydroxide (product code EJK), Class II - Special Controls.

Submitted by Neodental Chemical Products Co., Ltd. (Austin, US). The FDA issued a Cleared decision on August 19, 2011 after a review of 66 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3250 - 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 Neodental Chemical Products Co., Ltd. devices

FDA 510(k) Submission Details - K111668

510(k) Number K111668 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 14, 2011
Decision Date August 19, 2011
Days to Decision 66 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
61d faster than avg
Panel avg: 127d · This submission: 66d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EJK Device Classification - Class 2, Special Controls

Product Code EJK Liner, Cavity, Calcium Hydroxide
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3250
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 - EJK Liner, Cavity, Calcium Hydroxide

All 56
Devices cleared under the same product code (EJK) and FDA review panel - the closest regulatory comparables to K111668.
TEETHMATE DESENSITZER SET TEETHMATE DESENSITIZER POWDER TEETHMATE DESENSITIZER LIQUID
K122421 · Kuraray Noritake Dental, Inc. · Dec 2012
NUCAL
K120003 · Pulpdent Corporation · Apr 2012
LIME-LITE II
K113711 · Pulpdent Corporation · Mar 2012
THERACAL LC
K063237 · Bisco, Inc. · Dec 2006
APEXCAL
K060365 · Ivoclar Vivadent, Inc. · Apr 2006
BISBLOCK
K033521 · Bisco, Inc. · Jan 2004