TITAN DENTAL IMPLANT SYSTEM
K-Number: K042971 · 2005-01-14
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Device Summary
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
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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