ClearanceBrief
Company · FR

Fci (France Chirurgie Instrumentation) Sas

FDA 510(k) clearances and medical device recalls filed under this name, 2012 to 2022. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
OKSLacrimal Stents And Intubation Sets6
HPZImplant, Eye Sphere1
NCBWeights, Eyelid, Implantable1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 24, 2022K212741EZYPOR
Fci (France Chirurgie Instrumentation) Sas, FR
HPZ
Jun 11, 2021K203569Gold Tapered Weight Eyelid Implants, Platinum Tapered Weight Eyelid Implants
Fci (France Chirurgie Instrumentation) Sas, FR
NCB
Mar 11, 2021K201892Ritleng®+ and Ritleng®+ PVP
Fci (France Chirurgie Instrumentation) Sas, FR
OKS
Dec 18, 2020K201606LacriJet®
Fci (France Chirurgie Instrumentation) Sas, FR
OKS
Nov 3, 2016K161373Nunchaku
Fci (France Chirurgie Instrumentation), FR
OKS
Dec 4, 2013K130375SELF-RETAINING BICANALICULUS INTUBATON SET II
Fci Sas (France Chirurgie Instrumentation)
OKS
Aug 9, 2012K121142CRAWFORD BIOCANALICULUS INTUBATION
Fci Sas (France Chirurgie Instrumentation)
OKS
Aug 3, 2012K113536MASTERKA 40 MASTERKA 35 MASTERKA 30
Fci Sas (France Chirurgie Instrumentation)
OKS

Latest recalls

DateFirm and productCodeLinked 510(k)
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