Cleared Special

K100510 - CERAMIR CROWN & BRIDGE

K100510 is an FDA 510(k) clearance for CERAMIR CROWN & BRIDGE, manufactured by Doxa AB. The device is a Class 2 Dental device with product code EMA cleared through the Special 510(k) pathway after a 31-day FDA review.

K100510 · Doxa AB · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2010
Decision
31d
Days
Class 2
Risk

K100510 is an FDA 510(k) clearance for the CERAMIR CROWN & BRIDGE. Classified as Cement, Dental (product code EMA), Class II - Special Controls.

Submitted by Doxa AB (Uppsala, SE). The FDA issued a Cleared decision on March 25, 2010 after a review of 31 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3275 - the FDA dental device regulatory framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Doxa AB devices

FDA 510(k) Submission Details - K100510

510(k) Number K100510 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 22, 2010
Decision Date March 25, 2010
Days to Decision 31 days
Submission Type Special
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
96d faster than avg
Panel avg: 127d · This submission: 31d
Pathway characteristics
Modification to existing cleared device.

EMA Device Classification - Class 2, Special Controls

Product Code EMA Cement, Dental
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3275
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 - EMA Cement, Dental

All 387
Devices cleared under the same product code (EMA) and FDA review panel - the closest regulatory comparables to K100510.
RETRIEVE IMPLANT CEMENT
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UNICEM
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ESTEMP NE
K100290 · Spident Co., Ltd. · Feb 2010
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K093338 · Dmg USA, Inc. · Feb 2010
DC PROVI CEM ESTHETIC, ESTHETIC MULTI F, IMPLANT
K091735 · S & C Polymer GmbH · Sep 2009