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

Bioline Dental Implant System

FDA 510(k) K250872 · Bioline Dental Implant Systems, Ltd.

510(k) number
K250872
Device name
Bioline Dental Implant System
Applicant
Bioline Dental Implant Systems, 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

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 K250872
510(k)DeviceApplicantDecision date
K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.
K250806Dental Implant SystemA.B. Dental Devices , Ltd.
K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., 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
K252286BIORES Dental Implant SystemChengdu Besmile Medical Technology Co., Ltd.
K252585ZENEX Implant System_R-SystemIzenimplant Co., Ltd.

Building a 510(k) around this device type?

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.