57 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PERKINELMER 226 SAMPLE COLLECTION DEVICES
FDA 510(k)
FDA Class 2
·Clinical Chemistry
PINNACLE Hip Solutions
FDA UDI
DEPUY (IRELAND)·10603295520337·PINNACLE Hip Solutions DUAL MOBILITY LINER PINN...
KYPHON XPANDER II INFLATABLE BONE TAMP
FDA 510(k)
FDA Class 2
·Orthopedic
PRIMAGARD NONSTERILE FEMORAL ANGIOGRAPHY DRAPES (MODELS PM1-0136, PM1-0119, PM1-0142)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
G7 SCREW
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PBI·June 2, 2017
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 19, 2025
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
AVAN CMNTD SHELL SS 50MM
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LZO·April 24, 2026
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
MODULAR CUP SYSTEM, RIMCUP
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018
RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018
AVAN CMNTD SHELL SS 50MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·January 21, 2026
KYPHON XPANDER II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code HRX·March 7, 2018
AVAULTA PLUS BIOSYNTHETIC SUPPORT SYSTEM - POSTERIOR
FDA Adverse Event
Injury
·C.R. BARD, INC (COVINGTON)·Product code FTL·May 15, 2013
CAREFUSION T-BIRD SERIES
FDA Adverse Event
Malfunction
·CAREFUSION·Product code CBK·September 22, 2014
UNKNOWN DEPUY 28MM + 12 12/14 HEAD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWY·June 9, 2011
RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018