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FDA 510(k)

Implacil Implant System

K-Number: K183024 · 2020-02-13

Decision Date2020-02-13
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Implacil Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Implacil DE Bortoli Material Odontologico Ltda. It received FDA 510(k) clearance on 2020-02-13 under 510(k) number K183024. 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 Implacil Implant System?

Implacil Implant System is a medical device that received FDA 510(k) clearance on 2020-02-13. The listed applicant is Implacil DE Bortoli Material Odontologico Ltda. The 510(k) number is K183024.

When did Implacil Implant System receive FDA 510(k) clearance?

Implacil Implant System received FDA 510(k) clearance on 2020-02-13, under 510(k) number K183024.

Who is the listed applicant for Implacil Implant System?

The FDA 510(k) record lists Implacil DE Bortoli Material Odontologico Ltda as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Implacil Implant System?

The FDA product code for Implacil Implant System is DZE.

Other records listing Implacil DE Bortoli Material Odontologico Ltda as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: DZE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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