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

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HYCURE

FDA 510(k)
FDA Unclassified ·Unknown

VERTEX® Reconstruction System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00885074239248·BONE SCREW 6955506 4.5 X 6MM CORTICAL

Zuma

FDA UDI
Seaspine Orthopedics Corporation·10889981097066·Zuma Implant Tray

Coulmed

FDA UDI
Coulmed Products Group LLC·10810087350335·Standard Sterile Surgical Gown, with Towel, X-L...

Arthrex®

FDA UDI
ARTHREX, INC.·00888867062474·UNIVERS REVERS SPACER 36+6MM

ACCUCORE TELEMETRY, MODIFICATION

FDA 510(k)
FDA Class 2 ·Cardiovascular

LAPAROSCOPIC CHOLANGIOGRAM CATHETER KIT

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

REVERS 36MM CA ADAPTER ASSEMBLY

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HSD·April 8, 2024

24MM BASEPLATE, MODULAR

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·March 15, 2021

HUM INSERT S/36+6 TO FIT IN 36 CUP CONST

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·May 14, 2020

CAPSUREFIX NOVUS

FDA Adverse Event
Injury ·MPRI·Product code DTB·February 11, 2013

TENDRIL ST

FDA Adverse Event
Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2011

TLC STAPLER

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 24, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·October 29, 2009

HUM INSERT S/36+3 TO FIT IN 36 CUP CONST

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·May 20, 2020

36 +4 LAT/24 GLENOSPHERE

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·May 20, 2020

24MM BASEPLATE, MODULAR

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·May 20, 2020

5.5X28MM PERIPHERAL SCREW, LOCKING

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·May 20, 2020

5.5X16MM PERIPHERAL SCREW, LOCKING

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·May 20, 2020

UNIVERS REVERS SPACER 36+6MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·May 20, 2020