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FDA 510(k)

ALPHA-FILL, ALPHA-CEM, AND ALPHA-SILVER

K-Number: K903481 · 1990-12-17

Decision Date1990-12-17
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ALPHA-FILL, ALPHA-CEM, AND ALPHA-SILVER is the device name listed in this FDA 510(k) record. The listed applicant is Dental Foremost. It received FDA 510(k) clearance on 1990-12-17 under 510(k) number K903481. 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 ALPHA-FILL, ALPHA-CEM, AND ALPHA-SILVER?

ALPHA-FILL, ALPHA-CEM, AND ALPHA-SILVER is a medical device that received FDA 510(k) clearance on 1990-12-17. The listed applicant is Dental Foremost. The 510(k) number is K903481.

When did ALPHA-FILL, ALPHA-CEM, AND ALPHA-SILVER receive FDA 510(k) clearance?

ALPHA-FILL, ALPHA-CEM, AND ALPHA-SILVER received FDA 510(k) clearance on 1990-12-17, under 510(k) number K903481.

Who is the listed applicant for ALPHA-FILL, ALPHA-CEM, AND ALPHA-SILVER?

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

What is the FDA product code for ALPHA-FILL, ALPHA-CEM, AND ALPHA-SILVER?

The FDA product code for ALPHA-FILL, ALPHA-CEM, AND ALPHA-SILVER is EBF.

Related Clinical Trials

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.

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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