13 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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THERMOPLASTIC POLYETHYLENE EXAMINATION (TPE) GLOVE
FDA 510(k)
FDA Class 1
·General Hospital
BI-METRIC HIP SYSTEM
FDA UDI
Biomet Uk Ltd·00880304253025·
VEGA MEDICAL SUCTION EQUIPMENT, MODEL SU-01/SU-DC01
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CORTISOL ELISA
FDA 510(k)
FDA Class 2
·Clinical Chemistry
PENUMA IMPLANT
FDA Adverse Event
Injury
·INTERNATIONAL MEDICAL DEVICES, INC.·Product code MIB·October 7, 2019
TIBIAL INSERT FIXED SPHERE FLEX SIZE 2/14 MM R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·September 7, 2018
ADAPTA DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·October 10, 2014
QUADRA H FEMORAL STEM
FDA Adverse Event
MEDACTA INTERNATIONAL SA·Product code LZO·June 5, 2013
VISIAN ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Injury
·STAAR SURGICAL COMPANY·Product code HQL·July 14, 2011
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code HSD·January 9, 2024
EQUINOXE PRESERVE STEM 12MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·May 29, 2019
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·July 2, 2019
EQUINOXE REVERSE 46MM GLENOSPHERE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·October 2, 2024