FDA 510(k)

Neodent Implant System - Zirconia Implant System

K-Number: K231803 · 2023-12-13

ApplicantJJGC Indústria e Comércio de Materiais Dentários S.A.

Decision Date2023-12-13

Product CodeNHA

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

Neodent Implant System - Zirconia Implant System is a medical device manufactured by JJGC Indústria e Comércio de Materiais Dentários S.A.. It received FDA 510(k) clearance on 2023-12-13 under approval number K231803. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Neodent Implant System - Zirconia Implant System?

Neodent Implant System - Zirconia Implant System is a medical device that received FDA 510(k) clearance on 2023-12-13. It is manufactured by JJGC Indústria e Comércio de Materiais Dentários S.A.. The 510(k) number is K231803.

When was Neodent Implant System - Zirconia Implant System approved by the FDA?

Neodent Implant System - Zirconia Implant System received FDA 510(k) clearance on 2023-12-13, under approval number K231803.

What company makes Neodent Implant System - Zirconia Implant System?

Neodent Implant System - Zirconia Implant System is manufactured by JJGC Indústria e Comércio de Materiais Dentários S.A..

What is the FDA product code for Neodent Implant System - Zirconia Implant System?

The FDA product code for Neodent Implant System - Zirconia Implant System is NHA.

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Related PubMed Literature

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Other Devices by JJGC Indústria e Comércio de Materiais Dentários S.A.

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Official Source

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