23 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BIOABSORBABLE INTERFERENCE SCREW MEGAFIX
FDA 510(k)
FDA Class 2
·Orthopedic
Diamond D
FDA UDI
Keystone Industries·H66810131071·Denture Acrylic HC Dk Veined
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033455883·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033455982·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033455906·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033455852·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033455876·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033455869·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033455845·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970768·
M2376A DEVICELINK SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
R STENT BILIARY ENDOPROSTHESIS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BALL HEADS: MECTACER 01.29.213 BIOLOX DELTA CERAMIC BALL HEAD 12/14 Ø 40 SIZE M
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·June 15, 2022
RESTORE ULTRA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 16, 2012
SPRINT QUATTRO
FDA Adverse Event
Malfunction
·MPRI·Product code LWS·February 8, 2014
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·March 20, 2013
ASR ACETABULAR IMPLANT 58
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 24, 2011
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Death
·W.L. GORE & ASSOCIATES,INC·Product code MIH·March 14, 2008
RESTORE
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 11, 2022
ARROW OnControl Ported Aspiration System Tray, Sterile, Rx only, The Arrow OnControl Bone Marrow Aspiration System is intended for bone marrow aspiration of the iliac crest of adult and pediatric patients. The Arrow OnControl Bone Marrow Biopsy System is intended for bone marrow core biopsy of the anterior or posterior iliac crest of adult patients
FDA Enforcement
Class II
·Terminated·Teleflex Medical·December 7, 2016