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510(k) Predicate Database
FDA 510(k) ClearanceDZE

MegaGen Zygoma Dental Implant System

FDA 510(k) K251232 · Megagen Implant Co., Ltd.

Clearance details

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510(k) number
K251232
Device name
MegaGen Zygoma Dental Implant System
Applicant
Megagen Implant Co., Ltd.
Product code
DZE
Decision
Substantially Equivalent
Decision date
Device class
Class 2
Regulation number
872.3640
Advisory committee
DE
Medical specialty
Dental

Candidate predicate devices

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Other devices cleared under product code DZE form a screening cohort, not a predicate determination. Compare intended use, technological characteristics, performance evidence, labeling, and current legal-marketing status before selecting a predicate.

Candidate predicate devices for K251232
510(k)DeviceApplicantDecision date
K261392TriActive Dental Implant SystemParagon Implant Mfg., LLC
K260463ZEROS Dental Implant SystemZeros Co., Ltd.
K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.
K250806Dental Implant SystemA.B. Dental Devices , Ltd.
K260006INOSS SystemInosys, Inc.
K252731Promimic ZrP Surface Dental Implant; Promimic ZrP + HAnano Surface Dental ImplantPromimic AB
K252031Adin Long Dental Implant SystemAdin Dental Implant Systems , Ltd.
K253334ZENEX Implant System_Short (R-System)Izenimplant Co., Ltd.
K252168Straumann® BLC Implants - Indication WideningInstitut Straumann AG
K253493Dentis SQ-SL AXEL FixtureDentis Co., Ltd.
K252197Nobel Biocare S Series ImplantsNobel Biocare AB
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Assyro turns predicate research into a substantial-equivalence comparison and an eSTAR-ready 510(k) workflow, so predicate strategy, testing evidence, and labeling stay aligned before FDA review.

  • PubMed
  • ClinicalTrials.gov
  • FDA
  • Health Canada
  • EMA
  • ICH
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