Cleared Traditional

Dental Glass Ceramics (K233016) - FDA 510(k) Clearance

Class II Dental device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K233016 · Shenzhen Yurucheng Dental Materials Co., Ltd. · Dental device
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Dec 2023
Decision
90d
Days
Class 2
Risk

K233016 is an FDA 510(k) clearance for the Dental Glass Ceramics. Classified as Powder, Porcelain (product code EIH), Class II - Special Controls.

Submitted by Shenzhen Yurucheng Dental Materials Co., Ltd. (Kengzi Street Office, Pingshan District,, CN). The FDA issued a Cleared decision on December 21, 2023 after a review of 90 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 Shenzhen Yurucheng Dental Materials Co., Ltd. devices

Submission Details

510(k) Number K233016 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 22, 2023
Decision Date December 21, 2023
Days to Decision 90 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
37d faster than avg
Panel avg: 127d · This submission: 90d
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 Consultant

Guangzhou Junyi Information Technology Co., Ltd.
Shanfeng Jiang

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - EIH Powder, Porcelain

All 184
Devices cleared under the same product code (EIH) and FDA review panel - the closest regulatory comparables to K233016.
Dental Glass Ceramics
K232673 · Chengdu Besmile Medical Technology Co., Ltd. · Jan 2024
Dental Porcelain Powder
K232676 · Chengdu Besmile Medical Technology Co., Ltd. · Jan 2024
Zirconia Block
K233125 · Hangzhou Ivista Medical Devices Co., Ltd. · Jan 2024
Dental Glass Ceramics Blocks
K232438 · Aibodent Biotechnology Co., Ltd. · Dec 2023
Gradual Dental Zirconia Blank
K231687 · Liaoning Upcera Co., Ltd. · Sep 2023
Dental Lithium Disilicate Glass-Ceramic
K230487 · Fuzhou Rick Brown Biomaterials Co., Ltd. · Jul 2023