Cleared Traditional

K152004 - Nanova Universal Composite

K152004 is an FDA 510(k) clearance for Nanova Universal Composite, manufactured by Nanova Biomaterials, Inc.. The device is a Class 2 Dental device with product code EBF cleared through the Traditional 510(k) pathway after a 120-day FDA review.

K152004 · Nanova Biomaterials, Inc. · Dental device
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Nov 2015
Decision
120d
Days
Class 2
Risk

K152004 is an FDA 510(k) clearance for the Nanova Universal Composite. Classified as Material, Tooth Shade, Resin (product code EBF), Class II - Special Controls.

Submitted by Nanova Biomaterials, Inc. (Columbia, US). The FDA issued a Cleared decision on November 17, 2015 after a review of 120 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3690 - 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 Nanova Biomaterials, Inc. devices

FDA 510(k) Submission Details - K152004

510(k) Number K152004 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 20, 2015
Decision Date November 17, 2015
Days to Decision 120 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
7d faster than avg
Panel avg: 127d · This submission: 120d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EBF Device Classification - Class 2, Special Controls

Product Code EBF Material, Tooth Shade, Resin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3690
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 - EBF Material, Tooth Shade, Resin

All 646
Devices cleared under the same product code (EBF) and FDA review panel - the closest regulatory comparables to K152004.
Pulpdent Solo Flowable Composite with MCP
K153249 · Pulpdent Corporation · Apr 2016
BEAUTIFIL II Gingiva
K151700 · Shofu Dental Corporation · Mar 2016
BEAUTIFIL II Enamel
K151699 · Shofu Dental Corporation · Dec 2015
Admira Fusion x-tra
K151956 · Voco GmbH · Oct 2015
G-Fix
K151541 · GC America, Inc. · Oct 2015
Mosaic Universal Composite
K151094 · Ultradent Products, Inc. · Jul 2015