16 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VEIN-GOGH INSTRUMENT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04047872673204·LEVAMED STABILI-TRI ANKLE SUP BLU R IV
ACE
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950017485·RETRACTOR SURGICAL CURVED DOWN 14X70MM 8-1/2" 21CM
SOL-M™ Hypodermic Needle
FDA UDI
Sol-Millennium Medical, Inc.·00818392015232·Sterile hypodermic needles intended to inject f...
Pusher/Extender
FDA UDI
ELLIQUENCE, LLC·00846338001797·
TRANS1 AXIALIF PLUS
FDA 510(k)
FDA Class 2
·Orthopedic
CONTOUR MENISCUS ARROW, MODELS 541110, 541113, AND 541116
FDA 510(k)
FDA Class 2
·Orthopedic
600 ML TRANSFER BAG
FDA Adverse Event
Malfunction
·CHARTER MEDICAL·Product code KSR·July 15, 2007
PEN NDL 31GA 8MM 14BAG 700CAS JP
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·September 29, 2020
OSS POLY TIBIAL BUSHING
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·May 14, 2013
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·September 23, 2014
LIGASURE ATLAS HANDSWITCHING 37CM
FDA Adverse Event
Injury
·COVIDIEN LLC (SHANGHAI)·Product code GEI·May 25, 2011
MEDTRONIC ICD
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DXY·May 29, 2020
GMK REVISION TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·March 31, 2026
INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·July 21, 2021
Model Number L131, ESSENTIO DR EL MRI Pacemaker
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025