37 results
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27ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SYNTHES (USA) LCP MODULAR FOOT PLATES
FDA 510(k)
FDA Class 2
·Orthopedic
2.7MM TI CORTEX SCREW SLF-TPNG WITH T8 STARDRIVE RECESS 24MM
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HWC·February 28, 2023
CD HORIZON® Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00721902954665·CASE 7050110 CDHL 5.5 APIC DEROT INST
PULSE
FDA UDI
Nuvasive, Inc.·00887517973870·Pulse Spine Clamp, Medium
Orthex
FDA UDI
ORTHOPEDIATRICS CORP.·00841132143247·Ring, Half 110mm
HAEMONETICS ORTHOPAT
FDA UDI
HAEMONETICS CORPORATION·30812747017811·ORTHOPAT 110 VOLT (ENGLISH)
Arthrex®
FDA UDI
ARTHREX, INC.·00888867317116·LOW PROFILE CORTICAL SCW, TI, 5.0x110MM
MODIFICATION TO TRELEX MESH SURGICAL MESH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
POWDER-FREE NITRILE EXAMINATION GLOVES, WHITE
FDA 510(k)
FDA Class 1
·General Hospital
Squadron
FDA UDI
ALPHATEC SPINE, INC.·00811801034367·Squadron Blade, Right, 70 mm
Squadron
FDA UDI
ALPHATEC SPINE, INC.·00811801034138·Squadron Blade, Right, 80 mm
Squadron
FDA UDI
ALPHATEC SPINE, INC.·00811801033247·Squadron Blade, Right, 60 mm
Squadron
FDA UDI
ALPHATEC SPINE, INC.·00811801034121·Squadron Blade, Right, 50mm
SLEEPEASY
FDA Adverse Event
Injury
·RESPIRONICS INC.·Product code BZD·April 12, 2012
REMSTAR PLUS M-SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·May 6, 2010
REMSTAR M SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·November 25, 2009
M-SERIES DC POWER SUPPLY
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·May 25, 2012
Widex
FDA UDI
Widex A/S·05706069670394·Widex EVOKE E-XP (Clay brown ) 110, Telecoil, R...
Widex
FDA UDI
Widex A/S·05706069670387·Widex EVOKE E-XP (Light beige ) 110, Telecoil, ...
Widex
FDA UDI
Widex A/S·05706069670400·Widex EVOKE E-XP (Dark brown ) 110, Telecoil, R...