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FDA 510(k)

MAGNE-DENT

K-Number: K840600 · 1984-04-30

ApplicantMagne-Dent
Decision Date1984-04-30
Product CodeEGG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MAGNE-DENT is the device name listed in this FDA 510(k) record. The listed applicant is Magne-Dent. It received FDA 510(k) clearance on 1984-04-30 under 510(k) number K840600. The device is classified under product code EGG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNE-DENT?

MAGNE-DENT is a medical device that received FDA 510(k) clearance on 1984-04-30. The listed applicant is Magne-Dent. The 510(k) number is K840600.

When did MAGNE-DENT receive FDA 510(k) clearance?

MAGNE-DENT received FDA 510(k) clearance on 1984-04-30, under 510(k) number K840600.

Who is the listed applicant for MAGNE-DENT?

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

What is the FDA product code for MAGNE-DENT?

The FDA product code for MAGNE-DENT is EGG.

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Related Devices (Code: EGG)

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.

K990979STECO-TITANMAGNETICSSteco-System-Technik GmbH & CokgK950259COUPLING DEVICE FOR DENTAL PROSTHESISDr. Joseph E. Grasso, D.D.S.K925700ZEST ANCHOR ADVANCED GENERATIONZest Anchors, Inc.K915299COGAN CORP KITS OF DENTAL HAND INSTRUMENTSCogan Corp.K912435DENTAL CONNECTOR PRECISION ATTACHMENTMetalor Dental USA Corp.K912567CONICAST, INTRACAST, OMECASTMetalor Dental USA Corp.

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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