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