8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
EDLICH WOUND MANAGEMENT TRAY
FDA 510(k)
FDA Class 2
·General Hospital
LACTOSCREW
FDA UDI
Biomet Orthopedics, LLC·00880304420953·
LYME IGM MICROASSAY
FDA 510(k)
FDA Class 2
·Microbiology
SUNGLASSES STYLE #(70116)
FDA 510(k)
FDA Class 1
·Ophthalmic
ACRYSOF
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·November 19, 2010
ASR ACETABULAR IMPLANT 58
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·January 9, 2013
AUTOGEN
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 1, 2014
REF 905572, 5.5mm Lactoscrew Anchor,WI Maxbraid No Nd (Lactosorb L-15 resorbable copolymer ) Sterile, EO; Biomet Sports Medicine, Warsaw, IN Product Usage: The Biomet Sports Medicine Soft Tissue Anchoring Devices are resorbable repair devices used to attach soft tissue to bone.
FDA Recall
Terminated
·Biomet, Inc.·Product code HWC·January 25, 2012