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FDA 510(k)

AVINENT DENTAL IMPLANT SYSTEM

K-Number: K121873 · 2013-12-11

ApplicantAvinent Implant System S.L.
Decision Date2013-12-11
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AVINENT DENTAL IMPLANT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Avinent Implant System S.L.. It received FDA 510(k) clearance on 2013-12-11 under 510(k) number K121873. 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 AVINENT DENTAL IMPLANT SYSTEM?

AVINENT DENTAL IMPLANT SYSTEM is a medical device that received FDA 510(k) clearance on 2013-12-11. The listed applicant is Avinent Implant System S.L.. The 510(k) number is K121873.

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

AVINENT DENTAL IMPLANT SYSTEM received FDA 510(k) clearance on 2013-12-11, under 510(k) number K121873.

Who is the listed applicant for AVINENT DENTAL IMPLANT SYSTEM?

The FDA 510(k) record lists Avinent Implant System S.L. as the applicant. This does not by itself establish the device manufacturer.

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

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

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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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