20 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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