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Fournitures Hospitalieres Industrie

FDA Regulatory Profile

Fournitures Hospitalieres Industrie has 0 FDA recalls, 0 inspections, 24 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Jan 23, 2018

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances24Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K171789ARROW Reverse Porous GlenoidJan 23, 2018
K163148BePOD® Foot ScrewsSep 14, 2017
K163710BePOD® EZ Weil ScrewsSep 8, 2017
K162068ARROW Anatomical Porous glenoidApr 10, 2017
K170040BePOD Cannulated Arthrodesis ScrewsApr 4, 2017
K150568ARROW Humeral stems size 6 and 16Oct 29, 2015
K150463CalcaNail Orthopedic NailMay 22, 2015
K150471CalcaNail Orthopedic Arthrodesis NailMay 22, 2015
K142778ARROW Reverse Shoulder long keel and short keel glenoid baseMar 20, 2015
K120740COLS® FIXATION SYSTEMMar 5, 2013
K112193ARROW REVERSE SHOULDER SYSTEMJul 12, 2012
K113591COLS PEEKDec 22, 2011
K093599ARROW ANATOMICAL SHOULDER SYSTEMNov 24, 2010
K080974TLS FIXATION SYSTEMJul 1, 2008
K070617CANNULATED SCREWJun 14, 2007
K060367TENOLIGAug 9, 2006
K052058MODIFICATION TO: TITANIUM TELEGRAPH HUMERAL NAILAug 22, 2005
K050556ALUMINA HEADMay 11, 2005
K042035ALUMINA HEADNov 17, 2004
K042332TITANIUM TELEGRAPH HUMERAL NAILOct 7, 2004

FDA data resources