ClearanceBrief
Company · FR

Cousin Biotech Sas

FDA 510(k) clearances and medical device recalls filed under this name, 2007 to 2019. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FTLMesh, Surgical, Polymeric4
OWIBone Fixation Cerclage, Sublaminar2
MBIFastener, Fixation, Nondegradable, Soft Tissue1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 9, 2019K181086Cortical Fixation Systems
Cousin Biotech Sas, FR
MBI
Aug 29, 2018K181799ResCUBE™ Ligament Fixation System
Cousin Biotech Sas, FR
OWI
Apr 10, 2018K172206NAJA™ Ligament Correction System
Cousin Biotech Sas, FR
OWI
Sep 4, 2014K133889PREMIUM
Cousin Biotech Sas, FR
FTL
Jun 25, 2010K093196BIOMESH CA.B.S. 'AIR COMPOSITE, MODELS: CABST1R05T, CABSAIRC7, CABSAIRC09
Cousin Biotech Sas, FR
FTL
Jun 26, 2008K072962CABS'AIR
Cousin Biotech Sas, FR
FTL
Aug 22, 2007K0709184DDOME
Cousin Biotech
FTL

Latest recalls

DateFirm and productCodeLinked 510(k)
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