52 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Infrared Thermometer
FDA 510(k)
FDA Class 2
·General Hospital
BI-METRIC X-SERIES HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304182639·
BI-METRIC X-SERIES HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304182332·
BI-METRIC X-SERIES HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304182936·
InFix®
FDA UDI
ZIMMER SPINE, INC.·00889024331181·
DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code PQF·April 14, 2018
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197080583·COLLIER needleholder, fenestrated jaws
12,5 c...
Responsive Orthopedics Total Knee Arthroplasty System
FDA UDI
RESPONSIVE ORTHOPEDICS, LLC·00841973106975·TRIAL 90-SRK-180314 POLY PS 3X14MM
Tibial Trial Tray
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215062057·
SPINAL USA INTERBODY FUSION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
IMNS MEDACTA NAVIGATION SYSTEM,33.221000US
FDA 510(k)
FDA Class 2
·Neurology
M2A ACETABULAR SYSTEM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·April 19, 2017
M2A-38 58MM CUP NON FLARED
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·January 23, 2018
HUDSON RCI
FDA Adverse Event
Malfunction
·TELEFLEX INCORPORATED·Product code BTM·January 30, 2019
M2A-MAGNUM 52-60MM TPR INSRT-3
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·January 23, 2018
TITANIUM SCREW LOW PROFILE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBF·November 13, 2020
LYNX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 20, 2013
PROXIMATE** SKIN STAPLER 35 REGULAR
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDT·July 27, 2011
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE INC.·Product code LZG·October 15, 2014
M2A-MAGNUM PF CUP
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·October 3, 2018