Cleared Traditional

K093560 - UPCERA ZIRCONIA BLANKS

K093560 is an FDA 510(k) clearance for UPCERA ZIRCONIA BLANKS, manufactured by Shenyang Upcera Co., Ltd.. The device is a Class 2 Dental device with product code EIH cleared through the Traditional 510(k) pathway after a 71-day FDA review.

K093560 · Shenyang Upcera Co., Ltd. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 2010
Decision
71d
Days
Class 2
Risk

K093560 is an FDA 510(k) clearance for the UPCERA ZIRCONIA BLANKS. Classified as Powder, Porcelain (product code EIH), Class II - Special Controls.

Submitted by Shenyang Upcera Co., Ltd. (Austin, US). The FDA issued a Cleared decision on January 28, 2010 after a review of 71 days - a notably fast clearance cycle.

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: 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 Shenyang Upcera Co., Ltd. devices

FDA 510(k) Submission Details - K093560

510(k) Number K093560 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 18, 2009
Decision Date January 28, 2010
Days to Decision 71 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
56d faster than avg
Panel avg: 127d · This submission: 71d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EIH Device Classification - Class 2, Special Controls

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 308
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