43 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MEDPOR PLUS ORBITAL VOLUME REPLACEMENT IMPANT
FDA 510(k)
FDA Class 2
·Ophthalmic
BUSCH®, BNA®
FDA UDI
BUSCH & CO. GmbH & Co. KG·D8120213571·Carbide, cone round, bone cutter
CA 15-3 ASSAY FOR THE ADVIA CENTAUR SYSTEM
FDA 510(k)
FDA Class 2
·Immunology
MODIFICATION TO OMEGA 21 SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
TRANSEND GUIDEWIRE
FDA Adverse Event
Malfunction
·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP·Product code DQX·October 27, 2009
TRANSEND GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 7, 2010
TRANSEND GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010
TRANSEND GUIDEWIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·July 14, 2010
RINGLOC-X ARCOMXL H/W 50/32MM 23
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·May 10, 2016
WATCHMAN FLX LEFT ATRIAL APPENDAGE CLOSURE DEVICE WITH DELIVERY SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NGV·February 2, 2022
RINGLOC-X ARCOMXL H/W 54/36MM 24
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·July 1, 2016
RINGLOC-X ARCOM LINER
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·July 20, 2017
RINGLOC-X E1 H/W 60/36MM 26
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·July 20, 2016
RINGLOC-X E1 H/+3MM 50/36MM 23
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·February 1, 2016
ARCOM XL HI-WALL LINER RINGLOC-X SZ 46MM (RINGLOC SIZE 22)
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·July 29, 2016
TRANSEND GUIDEWIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·November 9, 2010
RINGLOC-X E1 H/W 60/36MM 26
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·July 20, 2016
ARCOM XL HI-WALL LINER RINGLOC-X SZ 54MM (RINGLOC SIZE 24)
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·April 20, 2016
ARCOM XL HI-WALL LINER RINGLOC-X SZ 46MM (RINGLOC SIZE 22)
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·July 29, 2016
ARCPM 1050 RESIN-HIPS
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·April 5, 2017