12 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CHARLOTTE 7.0 MULTI-USE COMPRESSION SCREW AND WASHER
FDA 510(k)
FDA Class 2
·Orthopedic
N/A
FDA UDI
GEORGE TIEMANN & CO.·B5820705250·FORCEPS
Paltop
FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290114694629·Single-Unit Digital Analog for Lab, inc. Screw
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197541251·RZ Tebbet Breast Retractor
70x25m...
ARTHREX TENODESIS SCREW 7MM, 8MM, 9MM
FDA 510(k)
FDA Class 2
·Orthopedic
HARDYDISK OFLOXACIN 5MCG
FDA 510(k)
FDA Class 2
·Microbiology
ASR ACETABULAR CUPS 56
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·April 22, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORP.·Product code LZG·March 29, 2011
BIORAPTOR 2.9 SUTURE ANCHOR W/ULTRABRAID
FDA Adverse Event
Malfunction
·SMITH & NEPHEW INC., ENDOSCOPY DIV.·Product code MBI·July 1, 2008
KYPHON KURVE BONE FILLER DEVICE 13GA
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO·Product code KIH·July 14, 2020
UNKNOWN BEARING
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·March 10, 2017
BIOMEDICUS MULTISTAGE FEMORAL VENOUS CANNULA
FDA Adverse Event
Injury
·PERFUSION SYSTEMS·Product code DWF·February 19, 2024