FDA 510(k)

Dental Implants OKTAGON Bone Level Tapered Design

K-Number: K170287 · 2017-05-24

Decision Date2017-05-24

Product CodeDZE

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

Dental Implants OKTAGON Bone Level Tapered Design is a medical device manufactured by Hager& Meisinger GmbH. It received FDA 510(k) clearance on 2017-05-24 under approval number K170287. 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 Dental Implants OKTAGON Bone Level Tapered Design?

Dental Implants OKTAGON Bone Level Tapered Design is a medical device that received FDA 510(k) clearance on 2017-05-24. It is manufactured by Hager& Meisinger GmbH. The 510(k) number is K170287.

When was Dental Implants OKTAGON Bone Level Tapered Design approved by the FDA?

Dental Implants OKTAGON Bone Level Tapered Design received FDA 510(k) clearance on 2017-05-24, under approval number K170287.

What company makes Dental Implants OKTAGON Bone Level Tapered Design?

Dental Implants OKTAGON Bone Level Tapered Design is manufactured by Hager& Meisinger GmbH.

What is the FDA product code for Dental Implants OKTAGON Bone Level Tapered Design?

The FDA product code for Dental Implants OKTAGON Bone Level Tapered Design is DZE.

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Other Devices by Hager& Meisinger GmbH

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Related Devices (Code: DZE)

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Official Source

View on FDA Database →

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