38 results · 44ms · 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.

CarboClear® Pedicle Screw System, CarboClear® II Pedicle Screw System

FDA 510(k)
FDA Class 2 ·Orthopedic

DJO SURGICAL

FDA UDI
Encore Medical, L.P.·00190446923091·SPECIAL EMPOWR KNEE 2 DEG VARUS, TIBIAL RECUT G...

Blade Handle

FDA UDI
KATENA PRODUCTS, INC.·00841668112373·CHUCK HANDLE #3KA 7.5CM LONG

AUROPAL 60

FDA 510(k)
FDA Class 2 ·Dental

VASCULAR GRAFT TUNNELER-STANDARD CURVE, MID CURVE, FULL CURVE, SHORT STANDARD CURVE, VASCULAR GRAFT TUNNELER ACCESSORIES

FDA 510(k)
FDA Class 2 ·Cardiovascular

ELLUME COVID-19 HOME TEST

FDA Adverse Event
Malfunction ·ELLUME LIMITED·Product code QKP·December 16, 2021

ENDOTAK DSP

FDA Adverse Event
Malfunction ·CARDIAC PACEMAKERS·Product code LWS·August 8, 2000

VALIANT CAPTIVIA UNK

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code MIH·December 18, 2019

VALIANT CAPTIVIA UNK

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code MIH·December 18, 2019

PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAW·October 30, 2020

VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·April 17, 2020

INSPIRE OXYGENATOR

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA·Product code DTZ·March 4, 2026

AXIOM REG IMPLANT

FDA Adverse Event
Injury ·ANTHOGYR·Product code DZE·September 13, 2019

AXIOM REG IMPLANT

FDA Adverse Event
Injury ·ANTHOGYR·Product code DZE·September 10, 2019

UNKNOWN ENDO GIA SULU

FDA Adverse Event
Injury ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·July 10, 2019

UNKNOWN ENDO GIA INSTRUMENT

FDA Adverse Event
Injury ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·July 10, 2019

AXIOM REG IMPLANT

FDA Adverse Event
Injury ·ANTHOGYR·Product code DZE·July 31, 2019

AXIOM REG IMPLANT

FDA Adverse Event
Injury ·ANTHOGYR·Product code DZE·September 11, 2019

MINICAP PD TRANSFER SET (EASY-LOCK) WITH TWIST CLAMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·October 21, 2008

SPRINT QUATTRO SECURE

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 11, 2011