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FDA 510(k)

FRIALIT-2 ESTHETICBASE ABUTMENT

K-Number: K013438 · 2001-12-20

ApplicantFriadent GmbH
Decision Date2001-12-20
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FRIALIT-2 ESTHETICBASE ABUTMENT is the device name listed in this FDA 510(k) record. The listed applicant is Friadent GmbH. It received FDA 510(k) clearance on 2001-12-20 under 510(k) number K013438. 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 FRIALIT-2 ESTHETICBASE ABUTMENT?

FRIALIT-2 ESTHETICBASE ABUTMENT is a medical device that received FDA 510(k) clearance on 2001-12-20. The listed applicant is Friadent GmbH. The 510(k) number is K013438.

When did FRIALIT-2 ESTHETICBASE ABUTMENT receive FDA 510(k) clearance?

FRIALIT-2 ESTHETICBASE ABUTMENT received FDA 510(k) clearance on 2001-12-20, under 510(k) number K013438.

Who is the listed applicant for FRIALIT-2 ESTHETICBASE ABUTMENT?

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 FRIALIT-2 ESTHETICBASE ABUTMENT?

The FDA product code for FRIALIT-2 ESTHETICBASE ABUTMENT is DZE.

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Other records listing Friadent GmbH as applicant

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Related Devices (Code: DZE)

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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

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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