Cleared Traditional

K192251 - Livento Press

K192251 is the FDA 510(k) clearance for Livento Press by Cendres & Metaux SA. It is a Class 2 Dental device (product code EIH) cleared through the Traditional 510(k) pathway after a 148-day FDA review.

K192251 · Cendres & Metaux SA · Dental device
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Jan 2020
Decision
148d
Days
Class 2
Risk

K192251 is an FDA 510(k) clearance for the Livento Press, Soprano 10, Soprano. Classified as Powder, Porcelain (product code EIH), Class II - Special Controls.

Submitted by Cendres & Metaux SA (Biel/Bienne, CH). The FDA issued a Cleared decision on January 15, 2020 after a review of 148 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6660 - 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 Cendres & Metaux SA devices

Submission Details

510(k) Number K192251 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 20, 2019
Decision Date January 15, 2020
Days to Decision 148 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
21d slower than avg
Panel avg: 127d · This submission: 148d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code EIH Powder, Porcelain
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.6660
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 - EIH Powder, Porcelain

All 260
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DD Contrast
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K191903 · Prismatik Dentalcraft, Inc. · Nov 2019