15 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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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
RINGLOC-X E1 H/W 60/36MM 26
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·July 20, 2016
OCTRODE PERCUTANEOUS LEAD
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·March 16, 2011
PFC STB 8MM SZ3
FDA Adverse Event
Injury
·DEPUY-RAYNHAM, A DIV OF DEPUY ORTHOPAEDICS, INC·Product code JWH·April 1, 2008
E1 HI-WALL LINER RINGLOC-X 60/36MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·March 7, 2017
RINGLOC-X E1 10DEG 54/32MM 24
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·October 31, 2017
E1 STANDARD +3MM LINER RINGLOC-X
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·May 18, 2017
RINGLOC-X E1 H/W 58/36MM 25
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·March 24, 2017
ARCOM XL HI-WALL LINER RINGLOC-X
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·September 7, 2017
RINGLOC-X E1 STD
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·May 19, 2017
RINGLOC-X E1 H/+3MM 50/36MM 23
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·December 18, 2015
RINGLOC-X ARCOMXL STD 58/36MM 25
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·February 24, 2016
E1 HI-WALL LINER RINGLOC-X 046MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·September 29, 2016