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FDA 510(k)

XIVE TG ABUTMENTS

K-Number: K032302 · 2003-10-02

ApplicantFriadent GmbH
Decision Date2003-10-02
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

XIVE TG ABUTMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Friadent GmbH. It received FDA 510(k) clearance on 2003-10-02 under 510(k) number K032302. 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 XIVE TG ABUTMENTS?

XIVE TG ABUTMENTS is a medical device that received FDA 510(k) clearance on 2003-10-02. The listed applicant is Friadent GmbH. The 510(k) number is K032302.

When did XIVE TG ABUTMENTS receive FDA 510(k) clearance?

XIVE TG ABUTMENTS received FDA 510(k) clearance on 2003-10-02, under 510(k) number K032302.

Who is the listed applicant for XIVE TG ABUTMENTS?

The FDA 510(k) record lists Friadent GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for XIVE TG ABUTMENTS?

The FDA product code for XIVE TG ABUTMENTS is DZE.

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Other records listing Friadent GmbH 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.

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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.

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