27 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Stryker Facial iD System
FDA 510(k)
FDA Class 2
·Dental
Ophthalmic Spatula
FDA UDI
KATENA PRODUCTS, INC.·00841668102534·KNOLLE LENS NUCLEUS SPATULA
SR-1000 Portable DR Imaging System, SR-1000S Portable DR Imaging System
FDA 510(k)
FDA Class 2
·Radiology
INFRARED SCIENCES BREASTSCAN IR SYSTEM
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
CADD
FDA Adverse Event
Malfunction
·ST PAUL·Product code FPA·June 1, 2022
CADD
FDA Adverse Event
Malfunction
·ST PAUL·Product code FPA·June 1, 2022
CADD
FDA Adverse Event
Malfunction
·ST PAUL·Product code FPA·June 1, 2022
CADD
FDA Adverse Event
Malfunction
·ST PAUL·Product code FPA·June 1, 2022
PORTEX BLUE LINE ULTRA CUFFED TRACHEOSTOMY TUBE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL INTERNATIONAL LTD.·Product code BTO·October 23, 2014
PINNACLE MTL INS NEUT36IDX52OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·August 18, 2011
TEN20 CONDUCTIVE PASTE
FDA Adverse Event
Injury
·D.O. WEAVER CO.·Product code GYB·December 10, 2012
CADD ADMINISTRATION SETS - FLOW STOP
FDA Adverse Event
Malfunction
·ST PAUL·Product code FPA·May 23, 2022
VGXP XP E1 TIB BRG RM 10X71
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MBH·May 29, 2015
VGXP XP E1 TIB BRG RL 10X71
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MBH·May 29, 2015
VANGUARD ANTERIOR STABILIZED TIBIAL BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·July 16, 2019
VANGUARD CRUCIATE RETAINING FEMORAL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·July 15, 2019
VANGUARD AS TIBIAL BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·July 19, 2019
BIOMET CC CRUCIATE TRAY
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBH·July 15, 2019
BIOMET MODULAR TIBIAL LOCKING BAR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·July 22, 2019
VANGUARD CR FEMORAL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·July 19, 2019