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FDA 510(k)

MODI. DICOR CASTABLE CERAMIC/ALL PORCELAIN BRIDGES

K-Number: K864725 · 1987-01-21

ApplicantDentsply Intl.
Decision Date1987-01-21
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MODI. DICOR CASTABLE CERAMIC/ALL PORCELAIN BRIDGES is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1987-01-21 under 510(k) number K864725. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODI. DICOR CASTABLE CERAMIC/ALL PORCELAIN BRIDGES?

MODI. DICOR CASTABLE CERAMIC/ALL PORCELAIN BRIDGES is a medical device that received FDA 510(k) clearance on 1987-01-21. The listed applicant is Dentsply Intl.. The 510(k) number is K864725.

When did MODI. DICOR CASTABLE CERAMIC/ALL PORCELAIN BRIDGES receive FDA 510(k) clearance?

MODI. DICOR CASTABLE CERAMIC/ALL PORCELAIN BRIDGES received FDA 510(k) clearance on 1987-01-21, under 510(k) number K864725.

Who is the listed applicant for MODI. DICOR CASTABLE CERAMIC/ALL PORCELAIN BRIDGES?

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 MODI. DICOR CASTABLE CERAMIC/ALL PORCELAIN BRIDGES?

The FDA product code for MODI. DICOR CASTABLE CERAMIC/ALL PORCELAIN BRIDGES is EMA.

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Related Devices (Code: EMA)

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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