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FDA 510(k)

VERICORE ABUTMENT IN ZIRCONIA FOR IMPLANT SYSTEMS

K-Number: K090976 · 2009-06-25

ApplicantWhip-Mix Corp.
Decision Date2009-06-25
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VERICORE ABUTMENT IN ZIRCONIA FOR IMPLANT SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Whip-Mix Corp.. It received FDA 510(k) clearance on 2009-06-25 under 510(k) number K090976. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERICORE ABUTMENT IN ZIRCONIA FOR IMPLANT SYSTEMS?

VERICORE ABUTMENT IN ZIRCONIA FOR IMPLANT SYSTEMS is a medical device that received FDA 510(k) clearance on 2009-06-25. The listed applicant is Whip-Mix Corp.. The 510(k) number is K090976.

When did VERICORE ABUTMENT IN ZIRCONIA FOR IMPLANT SYSTEMS receive FDA 510(k) clearance?

VERICORE ABUTMENT IN ZIRCONIA FOR IMPLANT SYSTEMS received FDA 510(k) clearance on 2009-06-25, under 510(k) number K090976.

Who is the listed applicant for VERICORE ABUTMENT IN ZIRCONIA FOR IMPLANT SYSTEMS?

The FDA 510(k) record lists Whip-Mix Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VERICORE ABUTMENT IN ZIRCONIA FOR IMPLANT SYSTEMS?

The FDA product code for VERICORE ABUTMENT IN ZIRCONIA FOR IMPLANT SYSTEMS is NHA.

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Other records listing Whip-Mix Corp. 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.

K092857VERICORE ABUTMENT IN TITANIUM FOR IMPLANT SYSTEMSK082299VERICORE IMPLANT ABUTMENTS

Related Devices (Code: NHA)

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.

K262207Cemented Plus AbutmentUnidental Co., Ltd.K260940BellaTek BarsZimVie US Corp, LLCK253999Universal Base ASC Engaging; Universal Base ASC Non-Engaging; Universal Base MUA ASC; Temporary Abutment Engaging and Non-Engaging; Healing Abutment Conical Connection; Omnigrip Clinical Screw Titanium; Omnigrip Prosthetic ScrewNobel Biocare ABK261147Neodent Implant System - NeoConvert FitJJGC Indústria e Comércio de Materiais Dentários S.A.K261122MIST ICImagine Milling Technologies, LLCK260061BioHorizons CEREC Compatible Ti-BasesBioHorizons Implant Systems, 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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