SILUX PLUS LIGHT CURED RESTORATIVE MATERIAL
K-Number: K872444 · 1987-09-11
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Device Summary
Frequently Asked Questions
What is the SILUX PLUS LIGHT CURED RESTORATIVE MATERIAL?
SILUX PLUS LIGHT CURED RESTORATIVE MATERIAL is a medical device that received FDA 510(k) clearance on 1987-09-11. The listed applicant is 3M Company. The 510(k) number is K872444.
When did SILUX PLUS LIGHT CURED RESTORATIVE MATERIAL receive FDA 510(k) clearance?
SILUX PLUS LIGHT CURED RESTORATIVE MATERIAL received FDA 510(k) clearance on 1987-09-11, under 510(k) number K872444.
Who is the listed applicant for SILUX PLUS LIGHT CURED RESTORATIVE MATERIAL?
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 PLUS LIGHT CURED RESTORATIVE MATERIAL?
The FDA product code for SILUX PLUS LIGHT CURED RESTORATIVE MATERIAL 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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