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FDA 510(k)

ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLE

K-Number: K093894 · 2010-03-03

ApplicantAnthogyr
Decision Date2010-03-03
Product CodeEFA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLE is the device name listed in this FDA 510(k) record. The listed applicant is Anthogyr. It received FDA 510(k) clearance on 2010-03-03 under 510(k) number K093894. The device is classified under product code EFA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLE?

ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLE is a medical device that received FDA 510(k) clearance on 2010-03-03. The listed applicant is Anthogyr. The 510(k) number is K093894.

When did ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLE receive FDA 510(k) clearance?

ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLE received FDA 510(k) clearance on 2010-03-03, under 510(k) number K093894.

Who is the listed applicant for ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLE?

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

What is the FDA product code for ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLE?

The FDA product code for ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLE is EFA.

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Other records listing Anthogyr 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.

K231072Anthogyr FlexiBase® titanium bases for Axiom® BLK233264Anthogyr INTEGRAL Guided Surgery CassettesK230104Anthogyr AXIOM® BL X3 implants, Anthogyr Multi-Unit components for AXIOM® BLK230680Anthogyr Surgical CassettesK160730Instrument kitsK090676MONTBLANC IMPLANTOLOGY AND OMNIPRATIQUE CONTRA-ANGLES

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Related Devices (Code: EFA)

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.

K192809Dental HandpieceMicro-Nx Co., Ltd.K163239SMARTmaticKaltenbach & Voigt GmbHK101172RDT3 HANDPIECE HEAD MODEL RDT3Redent Nova, Ltd.K092446INTRA LUX HEAD 3 LDSYKaltenbach & Voigt GmbH & Co.K090055LOW & HIGH SPEED KITDpm USA Corp.K092412STRONG IMPLANT HANDPIECESSaeshin Precision Co., Ltd.

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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