BIOBOND-CROWN & BRIDGE CERAMIC BONDING
K-Number: K760783 · 1976-10-15
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Device Summary
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.
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
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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