Cleared Traditional

K102635 - APOLONIA LASER IMPLANT SYSTEM

K102635 is an FDA 510(k) clearance for APOLONIA LASER IMPLANT SYSTEM, manufactured by Csm Implant Co., Ltd.. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 190-day FDA review.

K102635 · Csm Implant Co., Ltd. · Dental device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Mar 2011
Decision
190d
Days
Class 2
Risk

K102635 is an FDA 510(k) clearance for the APOLONIA LASER IMPLANT SYSTEM. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Csm Implant Co., Ltd. (Brea, US). The FDA issued a Cleared decision on March 22, 2011 after a review of 190 days - an extended review cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3640 - 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.

FDA 510(k) Submission Details - K102635

510(k) Number K102635 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 13, 2010
Decision Date March 22, 2011
Days to Decision 190 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
62d slower than avg
Panel avg: 128d · This submission: 190d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DZE Device Classification - Class 2, Special Controls

Product Code DZE Implant, Endosseous, Root-form
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3640
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 - DZE Implant, Endosseous, Root-form

All 1483
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K102635.
BLUE SKY BIO DENTAL IMPLANT SYSTEM
K102034 · Blue Sky Bio, LLC · Apr 2011
STRAIGHT ABUTMENT, 4.2, 4.6, 5.0, 6.4, IMPLANT 6.0, IMPLANT 7.0, IMPLANT 8.0 MODEL: 002061, 002062, 002063, 002064,
K101201 · Kat Implants, LLC · Apr 2011
OSSEOTITE II MODEL XIFOSSXXX
K100724 · Biomet 3i, Inc. · Apr 2011
ANTHOFIT OI, ANTHOFIT HE, OSSFIT AND AXIOM
K101913 · Anthogyr Sas · Mar 2011
ET III SA ULTRA WIDE SYSTEM
K103537 · Hiossen, Inc. · Mar 2011
ASTRA TECH IMPLANT SYSTEM
K101732 · Astra Tech AB · Feb 2011
K102635 · APOLONIA LASER IMPLANT SYSTEM
Download PDF FDA Summary Csm Implant Co., Ltd.