28 results · 32ms · Sources: EU EUDAMED, US FDA

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PHILIPS XRG 90 X-RAY GENERATOR SYSTEM

FDA 510(k)
FDA Class 1 ·Radiology

CAPSTONE SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

ACUNAV 90/10 DIAGNOSTIC ULTRASOUND CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

INTERSTIM II

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·May 25, 2012

HOLDING FORCEPS 170MM

FDA Adverse Event
Malfunction ·SYNTHES SALZBURG·Product code HTD·October 10, 2016

INTERSTIM II

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·October 30, 2012

INTERSTIM II

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 6, 2012

INTERSTIM II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO·Product code EZW·August 7, 2012

INTERSTIM II

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·August 17, 2012

INTERSTIM II

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·December 11, 2013

INTERSTIM II

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·August 20, 2014

ASR UNI FEMORAL IMPL SIZE 53

FDA Adverse Event
Injury ·Product code KWA·December 17, 2010

HAKIM VENTRICULAR & PERITONEAL CATHETERS WITH BACTISEAL

FDA Adverse Event
Injury ·CODMAN & SHURTLEFF, INC·Product code JXG·January 29, 2013

OT VERIO TEST STRIPS

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 15, 2014

PS TIBIAL INSERTS SZ 4, 9MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·April 14, 2023

CC FEMORAL SZ 3

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·October 10, 2024

CEMENTED FINNED TIB. TRA SZ 3F/3T

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·December 19, 2024

INTERSTIM II

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·November 26, 2014

OPTETRAK KNEE SYSTEM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·July 23, 2024

INTERSTIM II

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·April 8, 2013