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FDA 510(k)

SCALLOPED ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM

K-Number: K043190 · 2004-12-14

ApplicantInnova Life Sciences Corp.
Decision Date2004-12-14
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SCALLOPED ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Innova Life Sciences Corp.. It received FDA 510(k) clearance on 2004-12-14 under 510(k) number K043190. 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 SCALLOPED ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM?

SCALLOPED ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM is a medical device that received FDA 510(k) clearance on 2004-12-14. The listed applicant is Innova Life Sciences Corp.. The 510(k) number is K043190.

When did SCALLOPED ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM receive FDA 510(k) clearance?

SCALLOPED ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM received FDA 510(k) clearance on 2004-12-14, under 510(k) number K043190.

Who is the listed applicant for SCALLOPED ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM?

The FDA 510(k) record lists Innova Life Sciences Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCALLOPED ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM?

The FDA product code for SCALLOPED ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM is NHA.

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 Innova Life Sciences 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.

K052951ENDOPORE ANATOMIC ENDOSSEOUS DENTAL IMPLANT SYSTEMK053242PITT-EASY DENTAL IMPLANT SYSTEMK0321405.0 X 5MM ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM

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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