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FDA 510(k)

DENTIN ADHESIVE

K-Number: K872907 · 1987-08-03

ApplicantDentsply Intl.
Decision Date1987-08-03
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTIN ADHESIVE is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1987-08-03 under 510(k) number K872907. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTIN ADHESIVE?

DENTIN ADHESIVE is a medical device that received FDA 510(k) clearance on 1987-08-03. The listed applicant is Dentsply Intl.. The 510(k) number is K872907.

When did DENTIN ADHESIVE receive FDA 510(k) clearance?

DENTIN ADHESIVE received FDA 510(k) clearance on 1987-08-03, under 510(k) number K872907.

Who is the listed applicant for DENTIN ADHESIVE?

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 DENTIN ADHESIVE?

The FDA product code for DENTIN ADHESIVE is EBF.

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Other records listing Dentsply Intl. as applicant

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Related Devices (Code: EBF)

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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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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