8 results
·
17ms
·
Sources: EU EUDAMED, US FDA
LOVE LOCKERS
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ICA PLASMA HDL AND LDL MEASUREMENT SYSTEM
FDA 510(k)
FDA Class 1
·Clinical Chemistry
CENTRICON CONCENTRATOR
FDA 510(k)
FDA Class 1
·Clinical Chemistry
TROJAN PLEASURE PACK LUBRICATED CONDOMS
FDA Adverse Event
Injury
·CHURCH & DWIGHT CO., INC.·Product code HIS·October 29, 2014
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 7, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MPRI·Product code DTB·August 8, 2014
TALENT THORACIC STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MIH·February 11, 2011
OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·October 13, 2021