3,637 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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iTEMPSHIELD
FDA 510(k)
FDA Class 2
·General Hospital
OptoMonitor 3
FDA UDI
Opsens Inc·07540184320103·
MEGA PLUS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809665580382·Rod(CoCr), Ø5.5 x 100mm
LEONE SPA
FDA UDI
LEONE SPA·08033707066804·ELASTIC LIGATURES TRANSP 1,0mm
Meridian
FDA UDI
Seaspine Orthopedics Corporation·10889981247386·No-Profile Interbody, 39mm x 30mm x 20mm, 10 Deg
SPEEDLOCK
FDA UDI
Smith & Nephew, Inc.·00817470002935·SPEEDLOCK HIP DRILL
Smith and Nephew
FDA UDI
Provision·B504OM2320100·
Sapphire NC ULTRA Coronary Dilatation Catheter
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955982323·
TSI Stem Broach
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215040451·
MABIS
FDA UDI
D-M-S HOLDINGS, INC.·00767056232013·CALIBER ANEROID GAUGE BLUE
SMARTSCREW II, MODELS 232010, 232012, 232014, 232016, 232018, 232020
FDA 510(k)
FDA Class 2
·Orthopedic
VIDAS C DIFFICILE GDH
FDA 510(k)
FDA Class 1
·Microbiology
GLOVETEX POWDER FREE NITRILE EXAMINATION GLOVES, BLUE, NON-STERILE
FDA 510(k)
FDA Class 1
·General Hospital
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·September 1, 2011
ROTATING MULTIPLE CLIP APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·November 6, 2014
DUROM US ACETABULAR COMPONENT 50/44 J
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·July 4, 2013
UNICEL DXC 600 SYNCHRON CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·August 19, 2011
Brand Name: Intermate Infusion Pump. Indicated for the intravenous administration of medications.
FDA Enforcement
Class II
·Terminated·Baxter Healthcare Corp.·July 3, 2013
OPTI-FREE REPLENISH
FDA Adverse Event
Injury
·ALCON - FORT WORTH / ALCON LABORATORIES, INC.·Product code LPN·September 3, 2010
OPTI-FREE REPLENISH
FDA Adverse Event
Injury
·ALCON - FORT WORTH / ALCON LABS INC·Product code LPN·September 1, 2010