FRIADENT PLUS DENTAL IMPLANT SYSTEMS
K-Number: K040170 · 2004-10-27
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Device Summary
Frequently Asked Questions
What is the FRIADENT PLUS DENTAL IMPLANT SYSTEMS?
FRIADENT PLUS DENTAL IMPLANT SYSTEMS is a medical device that received FDA 510(k) clearance on 2004-10-27. The listed applicant is Friadent GmbH. The 510(k) number is K040170.
When did FRIADENT PLUS DENTAL IMPLANT SYSTEMS receive FDA 510(k) clearance?
FRIADENT PLUS DENTAL IMPLANT SYSTEMS received FDA 510(k) clearance on 2004-10-27, under 510(k) number K040170.
Who is the listed applicant for FRIADENT PLUS DENTAL IMPLANT SYSTEMS?
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 FRIADENT PLUS DENTAL IMPLANT SYSTEMS?
The FDA product code for FRIADENT PLUS DENTAL IMPLANT SYSTEMS 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 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.
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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