24 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MECTALIF ANTERIOR
FDA 510(k)
FDA Class 2
·Orthopedic
MECTALIF ANTERIOR STAND-ALONE PLATE FLUSH H.12 MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code OVD·March 29, 2018
ALIF SCREWDRIVER UNIVERSAL JOINT
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code LXH·January 15, 2016
MECTALIF ANTERIOR SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code OVD·May 6, 2025
MECTALIF ANTERIOR TI-PEEK CAGE
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code OVD·January 4, 2018
CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 34mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665033601·
CN LOCK SCREW, F THREAD, Ø4.0MM X 34MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code KTW·June 12, 2024
RADIOGRAPHIC X-RAY SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
OCCLUFAST ROCK
FDA 510(k)
FDA Class 2
·Dental
UNK
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code KTW·September 12, 2025
CN LOCK SCREW, F THREAD, Ø4.0MM X 34MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code KTW·September 9, 2025
SONICATOR PLUS 994
FDA Adverse Event
Injury
·METTLER ELECTRONICS CORP.·Product code IPF·May 16, 2013
INTERMATE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code FRN·September 27, 2014
CAPSUREFIX
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 14, 2011
CN LOCK SCREW, F THREAD, Ø4.0MM X 34MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code KTW·April 4, 2024
CN LOCK SCREW, F THREAD, Ø4.0MM X 38MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code KTW·April 4, 2024
CN LOCK SCREW, F THREAD, Ø4.0MM X 36MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code KTW·April 4, 2024
CN LOCK SCREW, F THREAD, Ø4.0MM X 38MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code KTW·April 4, 2024
BD INSYTE¿ AUTOGUARD¿ BC SHIELDED IV CATHETER
FDA Adverse Event
Injury
·BECTON DICKINSON·Product code FOZ·September 26, 2023
CN LOCK SCREW, F THREAD, Ø4.0MM X 44MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KTW·March 3, 2025