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FDA 510(k)

SUPERFINE DIAMONDS

K-Number: K771214 · 1977-07-15

ApplicantDen-Mat Corp.
Decision Date1977-07-15
Product CodeEJL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SUPERFINE DIAMONDS is the device name listed in this FDA 510(k) record. The listed applicant is Den-Mat Corp.. It received FDA 510(k) clearance on 1977-07-15 under 510(k) number K771214. The device is classified under product code EJL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPERFINE DIAMONDS?

SUPERFINE DIAMONDS is a medical device that received FDA 510(k) clearance on 1977-07-15. The listed applicant is Den-Mat Corp.. The 510(k) number is K771214.

When did SUPERFINE DIAMONDS receive FDA 510(k) clearance?

SUPERFINE DIAMONDS received FDA 510(k) clearance on 1977-07-15, under 510(k) number K771214.

Who is the listed applicant for SUPERFINE DIAMONDS?

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

What is the FDA product code for SUPERFINE DIAMONDS?

The FDA product code for SUPERFINE DIAMONDS is EJL.

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Other records listing Den-Mat 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.

K9831061ST IMPRESSIONK895731DEN-MAT CERINATE PORCELAINK895269DEN-MAT LAMI-QUICKK881918LIGHT-CURED ZIONOMER CEMENTK875351DEN-MAT PORETCH (PORCELAIN ETCHANT)K872510DEN-MAT TENURE

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Related Devices (Code: EJL)

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.

K080687SMARTBURSS.S. White Burs, Inc.K071352CERADRILLGebr. Brasseler GmbH & Co. KGK061383BTI STERILE DENTAL DRILLS KIT, BTI ABUTMENTS AND CAPSB.T.I. Biotechnology Institute, Sl.K943273TRI HAWK BUR, FG BURTri Hawk Corp.K926205MONOSTERYLUtensili Super AbrasiviK923883DENTAL OR SURGICAL BURStratum Dental Technologies, 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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