14 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Dentis s-Clean Abutment Mini
FDA 510(k)
FDA Class 2
·Dental
Carbon
FDA UDI
Keystone Industries·H66842204400·FP3D Original Pink
NA
FDA UDI
DEPUY MITEK, LLC·10886705007257·Cortical Screw 4.5mm x 40mm
Blade Scalpel
FDA UDI
KATENA PRODUCTS, INC.·00841668113448·SUPER SHARPS 15 DEG 3MM (BX/5)
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613072773·Gerald Bayonet Bipolar Forcep 7 1/2" (190.5mm) ...
PRESTO BREAST BIOPSY DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
NEWCOR
FDA 510(k)
FDA Class 2
·Cardiovascular
RESTORE RECHARGABLE NEUROSTIMULATOR
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·October 31, 2008
LASIK
FDA Adverse Event
Injury
·Product code LZS·August 17, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 11, 2013
BIOMET KNEE SYSTEM MODULAR FINNED STEM WITH SCREW
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·July 21, 2017
VANGUARD CR FEMORAL COMPONENT
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·July 21, 2017
VANGUARD TIBIAL BEARING CR LIPPED
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·July 21, 2017
REGENEREX SERIES-A PATELLA 3 PEG
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MBH·July 21, 2017