18 results · 28ms · Sources: EU EUDAMED, US FDA

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Stat Profile Prime ES Comp Plus Analyzer System

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

LENSX LASER SYSTEM

FDA 510(k)
FDA Class 2 ·Ophthalmic

CRYOPATCH SG PULMONARY HEMI-ARTERY; TRUNK; BRANCH

FDA 510(k)
FDA Class 2 ·Cardiovascular

FEMORAL POSTERIOR AUGMENT CEMENTED

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

STEM EXTENSION STRAIGHT SPLINED UNCEMENTED

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

FEMORAL DISTAL AUGMENT CEMENTED

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

TIBIAL AUGMENT CEMENTED HALF BLOCK

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

FEMORAL DISTAL AUGMENT CEMENTED

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code MBH·August 17, 2022

TIBIAL AUGMENT CEMENTED HALF BLOCK

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code MBH·August 17, 2022

SEE H10 NARRATIVE

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 16, 2023

SEE H10 NARRATIVE

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 16, 2023

TIBIA FIXED CEMENTED LEFT SIZE D STEM EXTENSION

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 16, 2023

TIBIAL AUGMENT CEMENTED HALF BLOCK

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code MBH·August 17, 2022

COOK CELECT® PLATINUM NAVALIGN JUGULAR VENA CAVA FILTER SET

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·November 17, 2016

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 22, 2014

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 20, 2011

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·June 26, 2013

BIO-COMP SWIVELOCK C, CLD 5.5X19.1MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code MAI·April 22, 2020