31 results · 30ms · Sources: EU EUDAMED, US FDA

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GUMEASE DENTAL MOUTHPIECE

FDA 510(k)
FDA Class 2 ·Dental

Paltop

FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108699258·Titanium Base Abutment Round Anterior, Conical ...

Genius Total Knee System

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215023416·

Crescendo Meniscal Insert PS 17mm Size 2

FDA UDI
AMPLITUDE SAS·03701089525374·

SPEEDLINK TRANSVERSE CONNECTOR

FDA 510(k)
FDA Class 2 ·Orthopedic

OPTIBOND SOLO PLUS ACTIVATOR

FDA 510(k)
FDA Class 2 ·Dental

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·March 27, 2025

QUILL SRS

FDA Adverse Event
Malfunction ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·September 3, 2008

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·May 12, 2009

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·February 13, 2009

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 23, 2013

AMMONIA

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JIF·April 28, 2011

MAXIMO DR

FDA Adverse Event
Injury ·MEDTRONIC MED REL, INC.·Product code LWS·July 10, 2008

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP (DBA ANGIOTECH)·Product code NEW·March 15, 2010

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·August 24, 2009

QUILL KNOTLESS TISSUE-CLOSURE DEVICE

FDA Adverse Event
Injury ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·May 11, 2011

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·July 26, 2012

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 19, 2010

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·January 5, 2011

QUILL KNOTLESS TISSUE CLOSURE DEVICE

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·October 31, 2011