ClearanceBrief
Company ยท IT

Fin-Ceramica Faenza S.P.A.

FDA 510(k) clearances and medical device recalls filed under this name, 2016 to 2024. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GXNPlate, Cranioplasty, Preformed, Non-Alterable5

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 28, 2024K240567CustomizedBone Service
Fin-Ceramica Faenza S.P.A., IT
GXN
Jan 17, 2020K193547CustomizedBone Service
Fin-Ceramica Faenza S.P.A., IT
GXN
May 15, 2018K180513CustomizedBone Service
Fin-Ceramica Faenza S.P.A., IT
GXN
Sep 1, 2017K171507CustomizedBone Service
Fin-Ceramica Faenza S.P.A., IT
GXN
Dec 17, 2016K160707CustomizedBone Service
Fin-Ceramica Faenza S.P.A., IT
GXN

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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