Cleared Traditional

K101875 - BK BLANK MODEL 20,40,65,90

K101875 is an FDA 510(k) clearance for BK BLANK MODEL 20, manufactured by Bk Medent Co., Ltd.. The device is a Class 2 Dental device with product code EIH cleared through the Traditional 510(k) pathway after a 48-day FDA review.

K101875 · Bk Medent Co., Ltd. · Dental device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Aug 2010
Decision
48d
Days
Class 2
Risk

K101875 is an FDA 510(k) clearance for the BK BLANK MODEL 20,40,65,90. Classified as Powder, Porcelain (product code EIH), Class II - Special Controls.

Submitted by Bk Medent Co., Ltd. (Anaheim, US). The FDA issued a Cleared decision on August 23, 2010 after a review of 48 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.

FDA 510(k) Submission Details - K101875

510(k) Number K101875 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 06, 2010
Decision Date August 23, 2010
Days to Decision 48 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
80d faster than avg
Panel avg: 128d · This submission: 48d
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 482
Devices cleared under the same product code (EIH) and FDA review panel - the closest regulatory comparables to K101875.
FLUORCANASITE DENTAL CERAMIC
K100794 · Dr Sarah Pollington · Jan 2011
HASS ZIRTOOTH MODEL ZORTOOTH H. ZIRTOOTH T. ZIRTOOTHC, ZIRTOOTH P
K102305 · Hass Corp. · Dec 2010
ZIECON DISC WITH COLLAR FOR CAD/CAM MODEL ZD810-26, ZIECON BLOCK FOR MOM MODEL ZB763812-20, ZB653012-21, ZB402012-20, ZI
K102538 · Jyoti Ceramic Industries Private Limited · Oct 2010
NOBELPROCERA IPS E.MAX CROWN
K100512 · Nobel Biocare AB · Aug 2010
VITABLOCS
K102128 · Vita Zahnfabrik H.Rauter GmbH & Co. · Aug 2010
OBSIDIAN CERAMIC BLOCKS
K100781 · Prismatik Dentalcraft, Inc. · Jun 2010
K101875 · BK BLANK MODEL 20,40,65,90
Download PDF FDA Summary Bk Medent Co., Ltd.