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FDA 510(k)

Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants

K-Number: K193592 · 2020-04-28

Decision Date2020-04-28
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants is a medical device manufactured by Jjgc Industria E Comercio DE Materiais Dentarios S.A.. It received FDA 510(k) clearance on 2020-04-28 under approval number K193592. 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 Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants?

Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants is a medical device that received FDA 510(k) clearance on 2020-04-28. It is manufactured by Jjgc Industria E Comercio DE Materiais Dentarios S.A.. The 510(k) number is K193592.

When was Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants approved by the FDA?

Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants received FDA 510(k) clearance on 2020-04-28, under approval number K193592.

What company makes Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants?

Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants is manufactured by Jjgc Industria E Comercio DE Materiais Dentarios S.A..

What is the FDA product code for Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants?

The FDA product code for Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants is DZE.

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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.