34 results · 23ms · Sources: EU EUDAMED, US FDA

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CONFORMIS IUNI UNICONDYLAR KNEE REPLACEMENT SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

ArgenZ HT+ 98x10 A3

FDA UDI
ARGEN CORPORATION, THE·D818121974·Dental porcelain/ceramic restoration kit

MEDTRONIC MINIMED COMLINK, HARDWARE MODEL 7304 & SOFTWARE MODEL 7311

FDA 510(k)
FDA Class 2 ·General Hospital

ION HEALTH USB INSTA-SCAN THERMOMETER

FDA 510(k)
FDA Class 2 ·General Hospital

HISTOACRYL FLEXIBLE PACK 5

FDA Adverse Event
Injury ·B.BRAUN SURGICAL SA·Product code MPN·July 23, 2019

G7 SCREW

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

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·May 19, 2025

AVAN CMNTD SHELL SS 50MM

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

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

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

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code OYC·May 21, 2013

UNKNOWN

FDA Adverse Event
Other ·STRYKER MEDICAL·Product code FPO·June 3, 2011

TOTALCARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·August 13, 2008

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

DURAL ALPHA INSERT NEUTR JJ/36

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code LZO·February 18, 2026