Cleared Traditional

K122519 - DIO UF HSA INTERNAL SUB-MERGED IMPLANT ...

K122519 is an FDA 510(k) clearance for DIO UF HSA INTERNAL SUB-MERGED IMPLANT ..., manufactured by Dio Corporation. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 277-day FDA review.

K122519 · Dio Corporation · Dental device
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May 2013
Decision
277d
Days
Class 2
Risk

K122519 is an FDA 510(k) clearance for the DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEM. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Dio Corporation (Los Angeles, US). The FDA issued a Cleared decision on May 21, 2013 after a review of 277 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.

View all Dio Corporation devices

FDA 510(k) Submission Details - K122519

510(k) Number K122519 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 17, 2012
Decision Date May 21, 2013
Days to Decision 277 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
150d slower than avg
Panel avg: 127d · This submission: 277d
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 759
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K122519.
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ETII SA FIXTURE SYSTEM
K123471 · Hiossen, Inc. · Jul 2013
STRAUMANN DENTAL IMPLANT SYSTEM
K130222 · Straumann USA, LLC · Apr 2013
STRAUMANN DENTAL IMPLANT SYSTEM
K123784 · Straumann USA, LLC · Apr 2013
XPEED ANYRIDGE INTERNAL IMPLANT SYSTEM
K123870 · Megagen Implant Co., Ltd. · Mar 2013