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FDA 510(k)

AMERICAN DENTAL IMPLANT

K-Number: K042462 · 2004-09-21

ApplicantAmerican Dental Implant Corporation
Decision Date2004-09-21
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AMERICAN DENTAL IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is American Dental Implant Corporation. It received FDA 510(k) clearance on 2004-09-21 under 510(k) number K042462. 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 AMERICAN DENTAL IMPLANT?

AMERICAN DENTAL IMPLANT is a medical device that received FDA 510(k) clearance on 2004-09-21. The listed applicant is American Dental Implant Corporation. The 510(k) number is K042462.

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

AMERICAN DENTAL IMPLANT received FDA 510(k) clearance on 2004-09-21, under 510(k) number K042462.

Who is the listed applicant for AMERICAN DENTAL IMPLANT?

The FDA 510(k) record lists American Dental Implant Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMERICAN DENTAL IMPLANT?

The FDA product code for AMERICAN DENTAL IMPLANT 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.

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Other records listing American Dental Implant Corporation 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.

K080397AMERICAN DENTAL IMPLANT ABUTMENT SYSTEM

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.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.

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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