30 results · 26ms · Sources: EU EUDAMED, US FDA

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AURORA

FDA 510(k)
FDA Class 2 ·Radiology

GRADIA®

FDA UDI
Gc America Inc.·14548161296564·GRADIA® CORE Kit (1CORE Cartridge 10 mL (20 g),...

GRADIA®

FDA UDI
Gc America Inc.·D0470036511·GRADIA® CORE Kit (1CORE Cartridge 10 mL (20 g),...

LINK Instruments - Drills, reamers and saw blades

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575157662·Bone trephine - Endo Model Knee System

EX-CELL 301, CATALOG NO. 200-3651

FDA 510(k)
FDA Class 1 ·Hematology

BIO-RAD %CDT TIA

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

DETACH 18 AND DETACH 11, NEUROLOGICAL EMBOLIZATION COIL SYSTEM

FDA 510(k)
FDA Class 2 ·Neurology

HEPARIN LOCK FLUSH

FDA Adverse Event
Malfunction ·APP·Product code NZW·June 27, 2012

5.0MM FLEXIBLE SHAFT

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HTO·February 28, 2013

UNKNOWN ZIMMER KNEE

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JWH·February 23, 2011

ENDOSCOPIC MULTIFEED STAPLER - 360 ROTATION 20 TITANIUM STAPLES

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GCJ·February 14, 2008

BD 10ML SYRINGE LUER-LOK TIP

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·June 10, 2019

AUTOSOFT 90

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·August 10, 2024

AUTOSOFT 90

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·August 10, 2024

AUTOSOFT 90

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·August 8, 2024

AUTOSOFT 90

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·August 8, 2024

AUTOSOFT 90

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·August 8, 2024

AUTOSOFT 90

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·August 8, 2024

AUTOSOFT 90

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·August 8, 2024

AUTOSOFT 90

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·August 8, 2024