20 results · 22ms · Sources: EU EUDAMED, US FDA

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Huvitz Imaging System

FDA 510(k)
FDA Class 2 ·Radiology

DD tempMED

FDA UDI
Dental Direkt GmbH·EDDIK116151·DD tempMED are pre-colored dental milling blank...

PIN SCREW

FDA UDI
BK MEDITECH CO.,LTD.·08809155855310·Wire Pin Screw, 2mm Shaft Diameter x 1.6mm Thre...

PIN SCREW

FDA UDI
BK MEDITECH CO.,LTD.·08809155855303·Wire Pin Screw, 2mm Shaft Diameter x 1.6mm Thre...

MED CONTOUR

FDA 510(k)
FDA Class 2 ·Physical Medicine

POWERWIRE RADIOFREQUENCY GUIDEWIRE

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

OT PING METER

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

GO BED PLUS

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·July 1, 2011

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 26, 2013

ThermaSure(TM), a CENORIN(TM) product, SERIES 1000 MEDICAL DEVICE DRYER: (a) Model 1009; (b) Model 1010 Forced air dryer for medical devices

FDA Enforcement
Class II ·Terminated·Cenorin, LLC·August 23, 2017