41 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DCCERAM SYSTEM
FDA 510(k)
FDA Class 2
·Dental
SimPro™ Now
FDA UDI
Wellspect AB·07392532188237·Single Use Urinary Catheter with water sachet. ...
CoRoent
FDA UDI
Nuvasive, Inc.·00887517575036·CoRoent Ant TLIF Ti, 14x11x40mm 0°
Oticon
FDA UDI
Oticon A/S·05707131271341·ALTA, KIT 10 WL OMNI 75 BE
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515019089·Carmalt Artery Fcps, cvd, 9"
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702563054·ELVAREX 2/KNEE HIGH/PROFILE-CLOSED TOE/DOTTED 5...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702537185·E1/AG/SL-OT/NOP5-T-OH-ZI/BL
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197398657·Micro Curette
bayone...
LOCKING COMPRESSION PLATE
FDA 510(k)
FDA Class 2
·Orthopedic
FORTIFIER DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL LF-01
FDA 510(k)
FDA Class 2
·Cardiovascular
T:SLIM G5 SYSTEM
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OYC·July 9, 2019
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 5, 2025
GORE® EXCLUDER® AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·September 5, 2014
GORE® EXCLUDER® AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·January 29, 2015
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·September 3, 2008
MEDISENSE OPTIUM
FDA Adverse Event
Malfunction
·Product code NBW·June 27, 2011
CR PROLONG 36MM BRNG STD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PHX·July 20, 2021
LOGIC CR TIB INSERT SLOPE++, SZ 3, 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·September 5, 2024
25MM VERSA-DIAL TAPER ADAPTOR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PHX·July 20, 2021