34 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CONFORMIS IUNI UNICONDYLAR KNEE REPLACEMENT SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ArgenZ HT+ 98x10 A3
FDA UDI
ARGEN CORPORATION, THE·D818121974·Dental porcelain/ceramic restoration kit
MEDTRONIC MINIMED COMLINK, HARDWARE MODEL 7304 & SOFTWARE MODEL 7311
FDA 510(k)
FDA Class 2
·General Hospital
ION HEALTH USB INSTA-SCAN THERMOMETER
FDA 510(k)
FDA Class 2
·General Hospital
HISTOACRYL FLEXIBLE PACK 5
FDA Adverse Event
Injury
·B.BRAUN SURGICAL SA·Product code MPN·July 23, 2019
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
AVAN CMNTD SHELL SS 50MM
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LZO·April 24, 2026
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
RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)
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
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·May 21, 2013
UNKNOWN
FDA Adverse Event
Other
·STRYKER MEDICAL·Product code FPO·June 3, 2011
TOTALCARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 13, 2008
RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018
G7 BONEMASTER LTD ACET SHL 58G
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code JDI·September 23, 2019
G7 FINNED BM 3 HOLE SHELL 48C
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code JDI·May 16, 2018
DURAL ALPHA INSERT NEUTR JJ/36
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code LZO·February 18, 2026