111 results
·
20ms
·
Sources: EU EUDAMED, US FDA
EZ-TRAXTM Persona Knee Containment Device
FDA 510(k)
FDA Class 2
·General Hospital
NA
FDA UDI
Smith & Nephew, Inc.·03596010543608·DYONICS 25 DAY TUBE SET MUST BE
...
Zavation
FDA UDI
Zavation LLC·00842166132597·Ti3Z CIF 13mmx15mmx7mm -10 deg
PMT® Halo Systems
FDA UDI
PMT CORPORATION·00650551110323·HALO, 1203-5 VEST PED00, COOLMAX LINER, 1211-1 ...
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193114385·HA PEEK EVOS Straight, ,7mmx11mmx 30mm , FLAT ...
Biliary Drainage Tube
FDA UDI
OLYMPUS MEDICAL SYSTEMS CORP.·04953170046940·Biliary Drainage Tube
TALOS®-C HA
FDA UDI
MEDITECH SPINE, LLC·B167522110070·
MIDWEST REPROCESSING CENTER REPROCESSED LNCS SESSORS; MIDWEST REPROCESSING CENTER REPROCESSED OXIMAX SENSORS; MIDWEST RE
FDA 510(k)
FDA Class 2
·Cardiovascular
TENODESIS SCREW, 5.5 MM, MODEL AR-1350-55
FDA 510(k)
FDA Class 2
·Orthopedic
GMK TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·October 22, 2025
LINOX SMART PROMRI S DX 65/17
FDA Adverse Event
Injury
·BIOTRONIK SE & CO. KG·Product code NVY·October 29, 2014
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·August 13, 2011
ACUITY
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·July 8, 2013
GMK TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·May 22, 2026
HERCULITE ULTRA
FDA Adverse Event
Injury
·KERR CORPORATION·Product code EBF·February 12, 2014
HERCULITE ULTRA
FDA Adverse Event
Injury
·KERR CORPORATION·Product code EBF·February 12, 2014
HERCULITE ULTRA
FDA Adverse Event
Injury
·KERR CORPORATION·Product code EBF·February 12, 2014
HERCULITE ULTRA
FDA Adverse Event
Injury
·KERR CORPORATION·Product code EBF·February 12, 2014
HERCULITE ULTRA
FDA Adverse Event
Injury
·KERR CORPORATION·Product code EBF·February 12, 2014
HERCULITE ULTRA
FDA Adverse Event
Injury
·KERR CORPORATION·Product code EBF·February 12, 2014