33 results · 29ms · Sources: EU EUDAMED, US FDA

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VEGA KNEE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

XPERT MRSA/SA BC (BLOOD CULTURE) ASSAY MODEL GXMRSA/SA-BC-10

FDA 510(k)
FDA Class 2 ·Microbiology

CROSSOVER CROSS CONNECTOR (ISOLA SPINAL SYSTEM)

FDA 510(k)
FDA Class 2 ·Orthopedic

G7 SCREW

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code PBI·June 2, 2017

VERTECEM V+ CEMENT KIT

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code NDN·March 28, 2013

AVAN CMNTD SHELL SS 50MM

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·April 24, 2026

VERTECEM V+ CEMENT KIT

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code NDN·February 27, 2013

MODULAR CUP SYSTEM, RIMCUP

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

AVAN CMNTD SHELL SS 50MM

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LZO·January 21, 2026

VERTECEM V+ CEMENT KIT

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code NDN·March 1, 2013

RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

V12 COVERED STENT

FDA Adverse Event
Injury ·ATRIUM MEDICAL CORP.·Product code JCT·May 15, 2013

RADIUS PROBE SHAFT T-HANDLE

FDA Adverse Event
Malfunction ·STRYKER SPINE-FRANCE·Product code LXH·September 26, 2014

TRAJECTORY GUIDE KIT, BIOPSY, EXTERNAL

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·May 23, 2011

RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

G7 BONEMASTER LTD ACET SHL 58G

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·September 23, 2019

G7 FINNED BM 3 HOLE SHELL 48C

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·May 16, 2018

VERTECEM V+ CEMENT KIT

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code NDN·February 27, 2013