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FDA 510(k)

TITAN DENTAL IMPLANT SYSTEM

K-Number: K042971 · 2005-01-14

Decision Date2005-01-14
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TITAN DENTAL IMPLANT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Titan Implants, Inc.. It received FDA 510(k) clearance on 2005-01-14 under 510(k) number K042971. 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 TITAN DENTAL IMPLANT SYSTEM?

TITAN DENTAL IMPLANT SYSTEM is a medical device that received FDA 510(k) clearance on 2005-01-14. The listed applicant is Titan Implants, Inc.. The 510(k) number is K042971.

When did TITAN DENTAL IMPLANT SYSTEM receive FDA 510(k) clearance?

TITAN DENTAL IMPLANT SYSTEM received FDA 510(k) clearance on 2005-01-14, under 510(k) number K042971.

Who is the listed applicant for TITAN DENTAL IMPLANT SYSTEM?

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

What is the FDA product code for TITAN DENTAL IMPLANT SYSTEM?

The FDA product code for TITAN DENTAL IMPLANT SYSTEM is DZE.

Related Clinical Trials

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.

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

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