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FDA 510(k)

DENTIN ADHESIVE

K-Number: K852024 · 1985-07-29

ApplicantDentsply Intl.
Decision Date1985-07-29
Product Code
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 1985-07-29 under 510(k) number K852024. 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 1985-07-29. The listed applicant is Dentsply Intl.. The 510(k) number is K852024.

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

DENTIN ADHESIVE received FDA 510(k) clearance on 1985-07-29, under 510(k) number K852024.

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.

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Other records listing Dentsply Intl. 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.

K123615IRIS - HIGH STRENGTH GLASS CERAMICK072730FRIADENT CERCON AND ANKYLOS CERCON BALANCE ABUTMENTSK070538XP BOND DUAL CURE UNIVERSAL TOTAL ETCH ADHESIVEK070019CARRARA VOLUMIAK061427PRE-IMPRESSION CONDITIONING SOLUTIONK052334CAVITRON RF ULTRASONIC SCALER SYSTEM WITH STERIMATE HANDPIECE, MODEL G-131

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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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