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Etex Corporation

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
6
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243609EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone )December 18, 2024
K182107CarriGen PFAugust 31, 2018
K132868CARRICELLFebruary 20, 2015
K141245ETEX MIXING AND DELIVERY SYSTEMJuly 9, 2014
K102812GAMMA-BSM; BETA-BSM; EQUIVABONEDecember 3, 2010