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FDA 510(k)

ST Internal Implant System

K-Number: K190919 · 2020-02-27

ApplicantT-Plus Implant Tech. Co., Ltd.
Decision Date2020-02-27
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ST Internal Implant System is a medical device manufactured by T-Plus Implant Tech. Co., Ltd.. It received FDA 510(k) clearance on 2020-02-27 under approval number K190919. 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 ST Internal Implant System?

ST Internal Implant System is a medical device that received FDA 510(k) clearance on 2020-02-27. It is manufactured by T-Plus Implant Tech. Co., Ltd.. The 510(k) number is K190919.

When was ST Internal Implant System approved by the FDA?

ST Internal Implant System received FDA 510(k) clearance on 2020-02-27, under approval number K190919.

What company makes ST Internal Implant System?

ST Internal Implant System is manufactured by T-Plus Implant Tech. Co., Ltd..

What is the FDA product code for ST Internal Implant System?

The FDA product code for ST Internal Implant System is DZE.

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Related PubMed Literature

PMID: 39892748 Long-term Safety and Performance of a Suprachoroidal Pressure Sensor System: Results of the EYEMATE-SC Trial Follow-up Study. Ophthalmology (2025) 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) PMID: 39726899 How to improve the mechanical safety of a novel spinal implant while saving costs and time. JOR spine (2024)

Other Devices by T-Plus Implant Tech. Co., Ltd.

K152787ST Internal Fixture System K152786A Plus Internal Fixture 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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