15 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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JOURNEY II CR KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
AF541
FDA UDI
Respironics, Inc.·00606959024724·AF541 Discharge Kit, 4 Point Headgear, Small/Me...
MaxFuse VBR, 10 (D) x 12 (W) x 54 (H)
FDA UDI
Pioneer Surgical Technology, Inc.·00846468055639·VBR, 10 (D) x 12 (W) x 54 (H)
56 SERIES JET NEBULIZER
FDA 510(k)
FDA Class 2
·Anesthesiology
X12 STERILE REFLECTIVE MARKER SPHERE
FDA 510(k)
FDA Class 2
·Neurology
Matrixx System
FDA UDI
NEXXT SPINE, LLC·00889929064771·Corpectomy, 12Dx14Wx43H 0°
Matrixx System
FDA UDI
NEXXT SPINE, LLC·00889929038871·Corpectomy, 12Dx14Wx43H 6°
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013
BLADELESS VP 5MM ST W/ FIXATION
FDA Adverse Event
Injury
·UNITED STATES SURGICAL·Product code GCJ·June 7, 2011
SCULPTRA
FDA Adverse Event
GLOBAL PHARMACOVIGILANCE AND EPIDEMIOLOGY/SANOFI-AVENTIS·Product code LMH·August 13, 2008
BONE SCR 6.5X25 SELF-TAP
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·November 29, 2022
BONE SCREW SELF-TAPPING 6.5 MM DIA. 50 MM LENGTH
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·November 29, 2022
BONE SCREW SELF-TAPPING 6.5 MM DIA. 20 MM LENGTH
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·November 29, 2022
BONE SCREW SELF-TAPPING 6.5 MM DIA. 20 MM LENGTH
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·November 29, 2022
BONE SCREW SELF-TAPPING 6.5 MM DIA. 40 MM LENGTH
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·November 29, 2022