30 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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COLLAGEN POWDER
FDA 510(k)
FDA Unclassified
·Unknown
GEN4 DIGITAL
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828112727·GEN4 DIGITAL
RINGLOC HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304229846·
VIABAHN ENDOPROSTHESIS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
FREEDLAND TENSION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
INFINION 16
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 19, 2021
32MM MOD HEAD COCR -3MM NECK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·July 21, 2017
ARCOMXL 32MM +3 MROM LNR SZ 22
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LZO·July 14, 2017
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·February 3, 2022
E1 RINGLOC ACETABULAR LINER 28MM SIZE 22 MAX-ROM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·December 19, 2016
STR MOD ACET INSERTER HANDLE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MDM·May 21, 2017
CARPENTIER-EDWARDS PERIMOUNT MAGNA EASE PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·Product code DYE·May 9, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·September 19, 2014
RHAPSODY +
FDA Adverse Event
Injury
·SORIN CRM·Product code NVZ·May 20, 2011
32MM MODULAR HEAD COCR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·October 24, 2017
ELECTRICAL VENOUS OCCLUDER (EVO)
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DXC·July 17, 2024
UNIVERSAL RINGLOC 2-HOLE SHELL
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·May 22, 2017
STR INSERTER 1/4-28 THRD KIT
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LXH·May 21, 2017
ECHO BIMETRIC STEM INSERTER
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LXH·January 26, 2018
TROCHANTERIC NAIL KIT, TI GAMMA3® Ø11X180MM X 125°
FDA Adverse Event
Injury
·STRYKER TRAUMA KIEL·Product code HSB·May 5, 2016