SILUX RESTORATIVE MATERIAL & ENAMEL BOND
K-Number: K810595 · 1981-03-24
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Device Summary
Frequently Asked Questions
What is the SILUX RESTORATIVE MATERIAL & ENAMEL BOND?
SILUX RESTORATIVE MATERIAL & ENAMEL BOND is a medical device that received FDA 510(k) clearance on 1981-03-24. The listed applicant is 3M Company. The 510(k) number is K810595.
When did SILUX RESTORATIVE MATERIAL & ENAMEL BOND receive FDA 510(k) clearance?
SILUX RESTORATIVE MATERIAL & ENAMEL BOND received FDA 510(k) clearance on 1981-03-24, under 510(k) number K810595.
Who is the listed applicant for SILUX RESTORATIVE MATERIAL & ENAMEL BOND?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SILUX RESTORATIVE MATERIAL & ENAMEL BOND?
The FDA product code for SILUX RESTORATIVE MATERIAL & ENAMEL BOND 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.
Other records listing 3M Company 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: 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
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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