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FDA 510(k)

Implant-One System

K-Number: K173701 · 2018-11-29

Decision Date2018-11-29
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Implant-One System is the device name listed in this FDA 510(k) record. The listed applicant is Implant Logistics, Inc.. It received FDA 510(k) clearance on 2018-11-29 under 510(k) number K173701. 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 Implant-One System?

Implant-One System is a medical device that received FDA 510(k) clearance on 2018-11-29. The listed applicant is Implant Logistics, Inc.. The 510(k) number is K173701.

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

Implant-One System received FDA 510(k) clearance on 2018-11-29, under 510(k) number K173701.

Who is the listed applicant for Implant-One System?

The FDA 510(k) record lists Implant Logistics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Implant-One System?

The FDA product code for Implant-One System is DZE.

Other records listing Implant Logistics, Inc. 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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