Cleared Traditional

K132725 - JUVORA DENTQAL DISC

K132725 is an FDA 510(k) clearance for JUVORA DENTQAL DISC, manufactured by Juvora. The device is a Class 2 Dental device with product code EBI cleared through the Traditional 510(k) pathway after a 146-day FDA review.

K132725 · Juvora · Dental device
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Jan 2014
Decision
146d
Days
Class 2
Risk

K132725 is an FDA 510(k) clearance for the JUVORA DENTQAL DISC. Classified as Resin, Denture, Relining, Repairing, Rebasing (product code EBI), Class II - Special Controls.

Submitted by Juvora (Thornton-Cleveleys, Lancashire, GB). The FDA issued a Cleared decision on January 23, 2014 after a review of 146 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3760 - 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 Juvora devices

FDA 510(k) Submission Details - K132725

510(k) Number K132725 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 30, 2013
Decision Date January 23, 2014
Days to Decision 146 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
19d slower than avg
Panel avg: 127d · This submission: 146d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EBI Device Classification - Class 2, Special Controls

Product Code EBI Resin, Denture, Relining, Repairing, Rebasing
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3760
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 - EBI Resin, Denture, Relining, Repairing, Rebasing

All 176
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