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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

POWDER FREE PURPLE NITRILE EXAMINATION GLOVES, NONSTERILE

FDA 510(k)
FDA Class 1 ·General Hospital

Atos Medical Inc.

FDA UDI
ATOS MEDICAL INC.·00817126020979·2010-072 Laryngectomy Pulmonary Kit with Standa...

TO BE ASSIGNED

FDA UDI
FGX INTERNATIONAL INC.·00193033380284·

Ocata Anterior Cervical System

FDA UDI
Kalitec Direct LLC·B07308K0100020·Caddie, Screws

TO BE ASSIGNED

FDA UDI
FGX INTERNATIONAL INC.·00193033380246·

InTess C Cervical Cage System

FDA UDI
Kalitec Direct LLC·B07309K0100020·Impactor Head, Modular, InTess C

Kalitec Special

FDA UDI
Kalitec Direct LLC·B073DRK0100020·Tap, 4.5mm Cann, Quarter Square

TO BE ASSIGNED

FDA UDI
FGX INTERNATIONAL INC.·00193033380260·

TO BE ASSIGNED

FDA UDI
FGX INTERNATIONAL INC.·00193033380253·

TO BE ASSIGNED

FDA UDI
FGX INTERNATIONAL INC.·00193033380277·

TO BE ASSIGNED

FDA UDI
FGX INTERNATIONAL INC.·00193033380291·

MATIRA ANTERIOR CERVICAL SYSTEM

FDA UDI
Kalitec Direct LLC·B07307K0100020·Caddie, 1-3 Level Plates

Kalitec Special

FDA UDI
Kalitec Direct LLC·B073DRK0100120·Counter Torque, Offset

DORNIER MEDILAS D SKINPULSE

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

CONTOUR POLARIS URETERAL STENT

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

FEMORAL ARRAY POST ASSEMBLY

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·February 18, 2020

POLARIS ULTRA

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FAD·June 27, 2019

AXSYM DIGOXIN III

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013

ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·February 11, 2011