35 results · 22ms · 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.

CD HORIZON SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

Per-Q-Cath

FDA UDI
Bard Access Systems, Inc.·00801741127694·Catheter Placement Kit

CUSTOM PROCEDURE KIT

FDA UDI
MEDIVATORS INC.·40677964005723·The ENDO CARRY-ON Procedure Kit contains all of...

Lumalite

FDA UDI
PRYOR PRODUCTS·00761887002869·5-leg detach w support wheel

TUFF TT IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·February 20, 2025

TUFF TT IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·December 24, 2024

TUFF TT IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·April 16, 2025

RADIOTHERAPEUTICS RF 3000 RADIOFREQUENCY GENERATOR

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

MIDAS TOUCH LATEX EXAMINATION GLOVES-POWDERED

FDA 510(k)
FDA Class 1 ·General Hospital

TUFF TT IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·August 15, 2024

TUFF TT IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·February 20, 2025

TUFF TT IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·April 16, 2025

TRUEBALANCE

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·August 13, 2014

TUFF TT IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·November 18, 2025

Z.S.G.M. CUTTER 2:1 RATIO ( CAUTION: SHARP )

FDA Adverse Event
Malfunction ·ZIMMER SURGICAL, INC.·Product code FZW·January 13, 2023

ZIMMER SKIN GRAFT MESHER

FDA Adverse Event
Malfunction ·ZIMMER SURGICAL, INC.·Product code FZW·January 13, 2023

MECHANICAL WALKER, ROLLATOR

FDA Adverse Event
GOODBABY·Product code ITJ·March 12, 2013

INRATIO

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·February 2, 2011

GE OEC 9400

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·February 21, 2008

INSTINCT JAVA POLYAXIAL PEDICLE SCREW DG 40

FDA Adverse Event
Injury ·ZIMMER SPINE·Product code NKB·July 12, 2016