53 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BIOSPINE VBR SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
JOBST SensiFoot
FDA UDI
BSN MEDICAL, INC.·00035664108649·SENSFOOT 8-15 KH XL NA 1 EN FR ES
Leva® Anterior Interbody System
FDA UDI
Spine Wave, Inc.·10840642108194·Plate, 26 mm/30 mm (W) x 11 mm (H)
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306819131·Retractor, Jordan-Simpson, Right Angled, 1"
KYPHON XPANDER II INFLATABLE BONE TAMP
FDA 510(k)
FDA Class 2
·Orthopedic
ANALYST PANELS + ANALYTICAL TEST ROTOR
FDA 510(k)
FDA Class 2
·Clinical Chemistry
CAIMAN DISP.INSTR.NON ARTICUL. D: 5/360MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015
CAIMAN DISP. INSTR. NON ARTICUL. D:5/360 MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015
CAIMAN DISP.INSTR.NON ARTICUL. D:5/360MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015
CONTOUR
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE LLC·Product code NBW·December 14, 2012
CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code GEI·November 1, 2015
KYPHOPAK TRAY
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code HRX·May 24, 2021
KYPHON XPANDER II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO·Product code HRX·November 6, 2019
KYPHON XPANDER II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO·Product code HRX·April 5, 2021
KYPHON XPANDER II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO·Product code HRX·July 11, 2019
KYPHON XPANDER II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO·Product code HRX·August 31, 2019
KYPHON XPANDER II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code HRX·March 7, 2018
PINNACLE PELVIC FLOOR REPAIR KITS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·May 14, 2013
MINICAP
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·June 2, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 14, 2008