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FDA 510(k)

BR Type Implant System

K-Number: K171179 · 2018-02-09

ApplicantBiotem Co., Ltd.
Decision Date2018-02-09
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BR Type Implant System is a medical device manufactured by Biotem Co., Ltd.. It received FDA 510(k) clearance on 2018-02-09 under approval number K171179. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BR Type Implant System?

BR Type Implant System is a medical device that received FDA 510(k) clearance on 2018-02-09. It is manufactured by Biotem Co., Ltd.. The 510(k) number is K171179.

When was BR Type Implant System approved by the FDA?

BR Type Implant System received FDA 510(k) clearance on 2018-02-09, under approval number K171179.

What company makes BR Type Implant System?

BR Type Implant System is manufactured by Biotem Co., Ltd..

What is the FDA product code for BR Type Implant System?

The FDA product code for BR Type Implant System is DZE.

Related Clinical Trials

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Related PubMed Literature

PMID: 41966145 From Registry to Reality: Opportunities to Enhance Post-market Surveillance of High-Risk Medical Devices Comment on "Quality and Utility of European Cardiovascular and Orthopaedic Registries for the Regulatory Evaluation of Medical Device Safety and Performance Across the Implant Lifecycle: A Systematic Review". International journal of health policy and management (2025)

Other Devices by Biotem Co., Ltd.

K171185IR Type Implant System K171297AR_N Type Implant System K190641AR_N SLA Type Implant System K222142BR SLA Type Implant System K222144IR SLA Type Implant System

Related Devices (Code: DZE)

K160475Ritter Dental Implant SystemRitter Implants GmbH & Co. KG K161244s-Clean OneQ-SL Narrow Implant SystemDentis Co., Ltd. K163043Zeramex P6 Dental Implant SystemDentalpoint AG K161497Dental Implants and AbutmentsDitron Precision, Ltd. K153332ETIII SA Fixture System (O3.2mm)Hiossen, Inc. K151970KJ Mini Implant SystemKj Meditech Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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