15 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OSTEOMED FOOT PLATING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MIN-R 2 Cassette with MIN-R Screen
FDA UDI
CARESTREAM HEALTH, INC.·60889977091615·24X30CM MIN-R 2 CASS W/MIN-R SCR
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690199229·AK3 Congruent Insert Trial Size 6, 14mm
LEONE SPA
FDA UDI
LEONE SPA·08033707065906·EXTRAORAL ELASTICS 1/2" 14 oz
TALOS®-C
FDA UDI
MEDITECH SPINE, LLC·B1675091614070·
TALOS®-C
FDA UDI
MEDITECH SPINE, LLC·B1675091614000·
NITINOL TC ELECTRODE
FDA Adverse Event
Malfunction
·COSMAN MEDICAL·Product code GXI·August 11, 2017
TALOS®-C
FDA UDI
MEDITECH SPINE, LLC·B167509161400A0·
TALOS®-C
FDA UDI
MEDITECH SPINE, LLC·B167509161407A0·
STRYKER TRAUMA PELVIC SET
FDA 510(k)
FDA Class 2
·Orthopedic
DIGITAL CLINICAL THERMOMETER, MODEL ACT 3020
FDA 510(k)
FDA Class 2
·General Hospital
EQUINOXE CAGE GLENOID L, POST AUG, RIGHT
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·May 7, 2024
CORTSCR Ø1.5 SELF-TAP L16 TAN
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code MQN·May 3, 2013
MINICAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·September 16, 2014
PENTA SURGICAL LEAD
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·April 28, 2011