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FDA 510(k)

CURASAN OSSEOLIVE DENTAL

K-Number: K111105 · 2012-12-20

ApplicantCurasan AG
Decision Date2012-12-20
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CURASAN OSSEOLIVE DENTAL is the device name listed in this FDA 510(k) record. The listed applicant is Curasan AG. It received FDA 510(k) clearance on 2012-12-20 under 510(k) number K111105. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURASAN OSSEOLIVE DENTAL?

CURASAN OSSEOLIVE DENTAL is a medical device that received FDA 510(k) clearance on 2012-12-20. The listed applicant is Curasan AG. The 510(k) number is K111105.

When did CURASAN OSSEOLIVE DENTAL receive FDA 510(k) clearance?

CURASAN OSSEOLIVE DENTAL received FDA 510(k) clearance on 2012-12-20, under 510(k) number K111105.

Who is the listed applicant for CURASAN OSSEOLIVE DENTAL?

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

What is the FDA product code for CURASAN OSSEOLIVE DENTAL?

The FDA product code for CURASAN OSSEOLIVE DENTAL is LYC.

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Related Devices (Code: LYC)

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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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