7 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TRF
FDA 510(k)
FDA Class 2
·Immunology
Sklar
FDA UDI
SKLAR CORPORATION·10649111450167·ANIS NH STR W/LK X-DEL
PHENIX CERVICAL INTERBODY DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
Boston ES (enflufocon A) Rigid Gas Permeable Contact Lens; Boston EO (enflufocon B) Rigid Gas Permeable Contact Lens; Boston XO (hexafocon A) Rigid Gas Permeable Contact Lens; Boston XO2 (hexafocon B) Rigid Gas Permeable Contact Lens
FDA 510(k)
FDA Class 2
·Ophthalmic
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORP·Product code MKJ·January 31, 2013
ASR ACETABULAR CUPS 52
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 31, 2011
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·July 3, 2014