45 results · 21ms · 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.

HARDYDISK, VANCOMYCIN 30MCG

FDA 510(k)
FDA Class 2 ·Microbiology

Sledgehammer

FDA UDI
Keystone Industries·H66810005091·SC 25 lb Pwd Light Red Pink

PowerPICC

FDA UDI
Bard Access Systems, Inc.·00801741101038·Catheter Placement Kit

OmniStand

FDA UDI
medica - Medizintechnik GmbH·04041925002805·Exerciser, non-measuring for stroke rehabilitation

VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·March 20, 2024

DOSE 1

FDA 510(k)
FDA Class 2 ·Radiology

SPIRAL RADIUS RODDING SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

Capture High Torque Screw System

FDA UDI
Smith & Nephew, Inc.·00885556822883·SCREW REMOVAL TOOL

CAPTURE™

FDA UDI
Ascension Orthopedics, Inc.·10381780247470·CAPTURE™ High Torque Screw System The screw rem...

CAPTURE™

FDA UDI
Ascension Orthopedics, Inc.·10381780247319·CAPTURE™ High Torque Screw System The screw rem...

Capture High Torque Screw System

FDA UDI
Smith & Nephew, Inc.·00885556822876·SCREW REMOVAL TOOL

CAPTURE™

FDA UDI
Ascension Orthopedics, Inc.·10381780247487·CAPTURE™ High Torque Screw System The screw rem...

Capture High Torque Screw System

FDA UDI
Smith & Nephew, Inc.·00885556824672·SCREW REMOVAL TOOL

SIG FEM ADPT TORQUE WRENCH

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·October 27, 2015

BD VACUTAINER® BUFF. NA CITRATE 0.109M, 3.2%

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY·Product code JKA·May 10, 2019

GMK-SPHERE FEMORAL COMPONENT SPHERE CEMENTED SIZE 5+ L

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 24, 2022

KNEE OTHER IMPLANT

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code HXC·August 24, 2016

SIG FEM ADPT TORQUE WRENCH

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·March 16, 2015

OBTRYX SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·March 12, 2013

X8000 LIGHTSOURCE

FDA Adverse Event
Malfunction ·STRYKER ENDOSCOPY SAN JOSE·Product code FCW·February 1, 2011