22 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KOALA TOCO
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Gyrus ACMI
FDA UDI
Gyrus ACMI, LLC·00821925016040·MCGEE PISTON SLIM, .6 MM DIAMETER 3.75 MM LENGT...
Suprasorb
FDA UDI
Huizhou Foryou Medical Devices Co., Ltd.·06940610115586·
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197540278·Caspar Rongeur upwards angled 3x12mm 160
mm
MICROVASCULAR ANASTOMOTIC DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
NUTRISAFE 2 FEEDING TUBES MODEL 362.XXX. 1362.XXX
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·August 26, 2019
ROD, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·February 6, 2019
5.5 TI CANNULATED TRANSLATION SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019
MAXISKY 440
FDA Adverse Event
Malfunction
·ARJOHUNTLEIGH MAGOG INC.·Product code FNG·May 24, 2013
SYNCHRON® SYSTEMS RHEUMATOID FACTOR (RF) REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code DHR·June 25, 2011
ORTHO SUMMIT SAMPLE HANDLING SYSTEM
FDA Adverse Event
Malfunction
·HAMILTON BONADUZ AG·Product code JTC·June 12, 2008
POLARIS SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code NKB·January 8, 2020
PEDICLE SCREW UNSPECIFIED
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021
PEDICLE SCREW UNSPECIFIED
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021
PEDICLE SCREW UNKNOWN TYPE/SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021
CANNULATED TRANSLATION SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code NKB·December 3, 2020
EQUINOXE SHOULDER COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWS·January 9, 2024
POLARIS TRANSLATION SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019