12 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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4F Infiniti Angiographic Catheter, 4F & 5F Nylex Angiography Catheters, 4F & 5F Tempo Angiography Catheters
FDA 510(k)
FDA Class 2
·Cardiovascular
PERMASHADE VENEER CEMENT
FDA 510(k)
FDA Class 2
·Dental
CARESTREAM DR LONG LENGTH IMAGING SYSTEM FOR DR 7500 SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
FREESTYLE LITE
FDA Adverse Event
Injury
·Product code NBW·October 4, 2012
MINIMAX CEMENTLESS ANATOMICAL STEM RIGHT SIZE 8
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·January 22, 2019
SHOULDER SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·July 28, 2025
RIATA ACTIVE FIXATION
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL INC., CRMD·Product code NVY·January 13, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011
REPLY
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA S.R.L.·Product code NVZ·June 14, 2013
SHOULDER SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·October 8, 2025
REVERSE SHOULDER SYSTEM GLENOID POLYAXIAL NON-LOCKING SCREW - L46
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·July 27, 2022
REVERSE SHOULDER SYSTEM HUMERAL REVERSE METAPHYSIS +0MM/0
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·March 9, 2021