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FDA 510(k)

MULTILINK IMPLANT

K-Number: K090704 · 2009-06-17

ApplicantIvoclar Vivadent, Inc.
Decision Date2009-06-17
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MULTILINK IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Ivoclar Vivadent, Inc.. It received FDA 510(k) clearance on 2009-06-17 under 510(k) number K090704. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTILINK IMPLANT?

MULTILINK IMPLANT is a medical device that received FDA 510(k) clearance on 2009-06-17. The listed applicant is Ivoclar Vivadent, Inc.. The 510(k) number is K090704.

When did MULTILINK IMPLANT receive FDA 510(k) clearance?

MULTILINK IMPLANT received FDA 510(k) clearance on 2009-06-17, under 510(k) number K090704.

Who is the listed applicant for MULTILINK IMPLANT?

The FDA 510(k) record lists Ivoclar Vivadent, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTILINK IMPLANT?

The FDA product code for MULTILINK IMPLANT is EBF.

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Other records listing Ivoclar Vivadent, Inc. as applicant

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Related Devices (Code: EBF)

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.

K262982Core·it DualSpident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261246SRGC-06GC America, 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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