22 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SomnoDent Avant
FDA 510(k)
FDA Class 2
·Dental
Vanguard Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304680579·
Vanguard Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304647817·
PRECISE SHP DIODE LASER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
21.3 INCH (54 CM) MONOCHROME LCD MONITOR MS23I2 (ML21023)
FDA 510(k)
FDA Class 2
·Radiology
TRUWAVE
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES DR·Product code DXO·April 22, 2026
VANGUARD CR FEMORAL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018
VANGUARD CR ILOK FEM-RT 65
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018
BIOMET CC I-BEAM TRAY 71MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018
UNKNOWN BIOMET ARCOM 3 PEG/POST SIZE 31
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018
ARCHITECT C8000 SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING, INC.·Product code JJE·October 3, 2008
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 22, 2013
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·July 28, 2011
TRUWAVE
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES DR·Product code DXO·March 27, 2025
VANGUARD UNKNOWN KNEE PATELLA
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018
BIOMET CC I-BEAM TRAY
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018
TRUWAVE
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES DR·Product code DXO·April 10, 2025
VANGUARD CR ILOK FEM-LT 65
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2019
SERIES A PAT STD 31 3 PEG
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2019
TRUWAVE
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES DR·Product code DXO·September 5, 2025