58 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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INSTRU-SAFE INSTRUMENT PROTECTION SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
BIOMET KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304002920·
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868558894·
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868248054·
3M™ Unitek™
FDA UDI
3M UNITEK CORPORATION·00652221037589·Unitek(TM) Bicuspid Band General Purpose Narrow...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613068462·Buck Ear Curette, Angled, Sharp, Size 0, 1.5mm ...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613068479·Buck Ear Curette, Angled, Sharp, Size 00, 1mm O...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613068486·Buck Ear Curette, Angled, Sharp, Size 1, 2mm Ou...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613068493·Buck Ear Curette, Angled, Sharp, Size 2, 2.5mm ...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613068509·Buck Ear Curette, Angled, Sharp, Size 3, 3mm Ou...
Verteloc Spinal System
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215129040·
CX50 DIAGNOSTIC ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
MULTIX FUSION
FDA 510(k)
FDA Class 2
·Radiology
MAXIM CONSTRAINED TIBIAL BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·April 16, 2018
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 5, 2025
MAXIM CONSTRAINED TIBIAL PLATE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·April 16, 2018
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013
STAB HIP PC 12-22 LG W/CS
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LZO·June 22, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·September 3, 2008
VNGD TI FEM CR 60MM LT
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·December 20, 2016