10 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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O. B. PACK IV
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
HOTWIRE™ RF GUIDEWIRE
FDA UDI
Atraverse Medical, Inc·00850057445572·The HOTWIRE™ is a sterile, single-use guidewire...
Rampart One Lumbar Interbody Fusion System
FDA UDI
SPINEOLOGY INC.·M7404902032·Rampart One Trial, 18mm, M, 16°
Invenio
FDA UDI
GRI Medical & Electronic Technology Co., Ltd.·16931918138329·Gown_Set-In sleeve_Standard_X-Large_Invenio Ext...
C02 LASER MULTIPULSE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BARD PERFIX LIGHT PLUG, MODELS 0117050, 0117060, 0117070, 0117080, 0117150, 0117160
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HOMECHOICE CYCLER-REFURBISHED
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·November 18, 2010
CORE UNIVERSAL DRIVER
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code ERL·November 26, 2012
GEMSTR 7 THPY ALT ST
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·May 7, 2014
STEALTHSTATION¿ S8 SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·October 17, 2025