15 results · 26ms · Sources: EU EUDAMED, US FDA

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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