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FDA 510(k)

J2A SLA Dental Implant System

K-Number: K161923 · 2017-11-09

Decision Date2017-11-09
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

J2A SLA Dental Implant System is a medical device manufactured by Kj Meditech Co., Ltd.. It received FDA 510(k) clearance on 2017-11-09 under approval number K161923. 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 J2A SLA Dental Implant System?

J2A SLA Dental Implant System is a medical device that received FDA 510(k) clearance on 2017-11-09. It is manufactured by Kj Meditech Co., Ltd.. The 510(k) number is K161923.

When was J2A SLA Dental Implant System approved by the FDA?

J2A SLA Dental Implant System received FDA 510(k) clearance on 2017-11-09, under approval number K161923.

What company makes J2A SLA Dental Implant System?

J2A SLA Dental Implant System is manufactured by Kj Meditech Co., Ltd..

What is the FDA product code for J2A SLA Dental Implant System?

The FDA product code for J2A SLA Dental Implant System is DZE.

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Official Source

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