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FDA 510(k)

BIOBOND-CROWN & BRIDGE CERAMIC BONDING

K-Number: K760783 · 1976-10-15

Decision Date1976-10-15
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BIOBOND-CROWN & BRIDGE CERAMIC BONDING is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1976-10-15 under 510(k) number K760783. The device is classified under product code EJS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOBOND-CROWN & BRIDGE CERAMIC BONDING?

BIOBOND-CROWN & BRIDGE CERAMIC BONDING is a medical device that received FDA 510(k) clearance on 1976-10-15. The listed applicant is Dentsply Intl.. The 510(k) number is K760783.

When did BIOBOND-CROWN & BRIDGE CERAMIC BONDING receive FDA 510(k) clearance?

BIOBOND-CROWN & BRIDGE CERAMIC BONDING received FDA 510(k) clearance on 1976-10-15, under 510(k) number K760783.

Who is the listed applicant for BIOBOND-CROWN & BRIDGE CERAMIC BONDING?

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 BIOBOND-CROWN & BRIDGE CERAMIC BONDING?

The FDA product code for BIOBOND-CROWN & BRIDGE CERAMIC BONDING is EJS.

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.

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.

View all 279 devices →

Related Devices (Code: EJS)

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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