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FDA 510(k)

NEW TRIAD TRANSHEET DENTURE BASE MATERIAL

K-Number: K905702 · 1991-04-29

ApplicantDentsply Intl.
Decision Date1991-04-29
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NEW TRIAD TRANSHEET DENTURE BASE MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1991-04-29 under 510(k) number K905702. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEW TRIAD TRANSHEET DENTURE BASE MATERIAL?

NEW TRIAD TRANSHEET DENTURE BASE MATERIAL is a medical device that received FDA 510(k) clearance on 1991-04-29. The listed applicant is Dentsply Intl.. The 510(k) number is K905702.

When did NEW TRIAD TRANSHEET DENTURE BASE MATERIAL receive FDA 510(k) clearance?

NEW TRIAD TRANSHEET DENTURE BASE MATERIAL received FDA 510(k) clearance on 1991-04-29, under 510(k) number K905702.

Who is the listed applicant for NEW TRIAD TRANSHEET DENTURE BASE MATERIAL?

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

What is the FDA product code for NEW TRIAD TRANSHEET DENTURE BASE MATERIAL?

The FDA product code for NEW TRIAD TRANSHEET DENTURE BASE MATERIAL is EBI.

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Related Devices (Code: EBI)

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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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