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

View full classification →

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
MegaGen Zygoma Dental Implant System
Dental Implant System
INOSS System
Promimic ZrP Surface Dental Implant; Promimic ZrP + HAnano Surface Dental Implant
Adin Long Dental Implant System
ZENEX Implant System_Short (R-System)
Straumann® BLC Implants - Indication Widening
Dentis SQ-SL AXEL Fixture
Nobel Biocare S Series Implants
BIORES Dental Implant System
ZENEX Implant System_R-System
GEN5™ and GEN5+™ 3.3mmD Dental Implants
NizPlant Dental Implant System
DIMPLO Implant System
Pterygoid Indication for GM Helix Implants
S.I.N. Tapered Pro Conical Zygoma Implant System
GEN5 and GEN5+ Dental Implant System
HexaPLUS S OneDrill Implant System
Paltop Dental Implant System
S.I.N. Dental Implant System
JDEvolution Plus L and JDEvolution Plus LE
NobelZygoma TiUltra Implant system
MIS C1 Implant System, MIS Seven Implant System, MIS M4 Implant System, MIS Lance+ Implant System, MIS Lance+ Conical Connection System
Neodent Implant System - Zirconia Implant System
S.I.N. Dental Implant System
Straumann® RidgeFit Implants
MIS LYNX Conical Connection Implant System
SD TL Implant System
DESS® Dental Implants
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

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.

Popular Product Codes

Commonly searched