Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: DZE FDA class 2

Implant, Endosseous, Root-Form

Dental

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The Endosseous Root-Form Implant is a dental implant surgically placed into the jawbone to serve as an artificial tooth root, upon which a crown, bridge, or denture is subsequently attached to restore missing teeth. It is classified as FDA Class 2, indicating moderate risk, and requires 510(k) clearance before marketing. The product code is DZE and the applicable regulation is 21 CFR 872.3640, under the Dental medical specialty. This device is an implant.

510(k) Clearances

50+ matches
K Number
Device Name
HEXIM Implant; Samwon General Abutments
URIS Long Implant & Abutments
T3 Pro Implants– ZimVie Packaging System
Bioline Dental Implant System
MBA Biotech Implant System
CeraRoot TL Implant System (TL)
OsseOne Dental Implant System
DAND Dental Implant System
SD Implant System
LONGY Implant and LONGY-N Implant
Surcam Dental Implant System
TRI-matrix® X-Force Implants
SD TL Implant System
BLUEDIAMOND IMPLANT
INNO SLA Mini Plus® Implant System
Alpha Dent Implants Dental Implants System
Quickdent Dental Implant System
Dental Implants and Abutments
Straumann® PURE Ceramic Implants
MIS LYNX Conical Connection Implant System
NUVENTUS NV.C™ Dental Implant System
LL Implant System
Accelx Implant System
Highness Implant System
ZENEX Implant System_Long
Immediate Molar Implants
JDZygoma dental implants
BTI Interna 3.0 Dental Implant System UnicCa®
DenQ Sub SLA Implant System
EK D3.3 and Ultra Wide Implants
Surgikor Fixation One, Abutment Blanks and Abutments
ICX-Implant System
Proimtech Dental Body Implant, Proimtech Abutment, Proimtech Healing Cap, Proimtech Abutment Screw
JDentalCare Dental Implant System: JDEvolution; JDEvolution plus; JDIcon; JDIcon plus
TOV Dental Implant System
LW Narrow Implant System
S.I.N. Dental Implant System
Prima Plus Conical Implant System
Conical Platform Dental Implants System
Tapered Pro Conical Implant System
S.I.N. Dental Implant System
8plant Implant System
Paltop Short Implants
Dentis s-Clean SQ-SL Fixture
Ticare Dental Implant Systems
Dental Implants and Abutments
NB Mini Implant System
Ni2 Implant System
External Hex Implant System
IS-III active Short Implant

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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