26 results · 24ms · Sources: EU EUDAMED, US FDA

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neon3™ universal OCT spinal stabilization

FDA 510(k)
FDA Class 2 ·Orthopedic

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B16721610320·

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B1672161032060·

ORTHOPEDIC SALVAGE SYSTEM (OSS)

FDA UDI
Biomet Orthopedics, LLC·00880304250932·

16PW - ACCO

FDA UDI
Certified Safety Manufacturing, Inc.·00766588110325·16PW - ACCO

ZEUS-T

FDA UDI
SPINAL ELEMENTS·00840916124113·Zeus-TLIF Implant, Size 16H x 10W x 32L

CARDO MEDICAL FEMORAL CEMENT RESTRICTOR, MODEL 503-MCRX

FDA 510(k)
FDA Class 2 ·Orthopedic

DEPOTONE

FDA 510(k)
FDA Class 2 ·General Hospital

CAPSUREFIX NOVUS

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 13, 2010

KYPHON XPEDE BONE CEMENT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·December 21, 2018

KYPHON XPEDE BONE CEMENT

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·May 29, 2019

KYPHON XPEDE BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·February 28, 2019

KYPHON XPEDE BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·February 28, 2019

1030489-2019-01511

FDA Adverse Event
Death ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NDN·December 31, 2019

LOGIC TIBIA PS MOD INSRT SZ 3 9MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·May 7, 2024

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

UNICEL DXC 800 SYNCHRON SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code JJE·June 17, 2011

ATTAIN OTW

FDA Adverse Event
Injury ·MPRI·Product code LWP·October 10, 2014

1030489-2019-01423

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code NDN·December 13, 2019

KYPHX® HV-R¿ BONE CEMENT

FDA Adverse Event
Malfunction ·CARDIAC SURGERY MFG KERKRADE·Product code NDN·September 8, 2021