18 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Digital Radiography CXDI-Pro, Digital Radiography D1
FDA 510(k)
FDA Class 2
·Radiology
NA
FDA UDI
Smith & Nephew, Inc.·03596010104298·4.0MM FULLY THREADED CANNULATED
...
AED
FDA UDI
NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657006743·Antrum Curette, forward cutting
Sklar®
FDA UDI
SKLAR CORPORATION·10649111204869·BROPHY SULLIVN STR SH SER 53/4
SLENDERTONE FLEX BOTTOM & THIGH TONING SYSTEM, TYPE 511
FDA 510(k)
FDA Class 2
·Physical Medicine
TL 04.1MM RN,S, SLACTIVE TIZR 6, 8, 10, 12, 14, 16MM DENTAL IMPLANTS
FDA 510(k)
FDA Class 2
·Dental
840 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·November 4, 2014
UNKNOWN SHOULDER
FDA Adverse Event
Other
·ENCORE MEDICAL, L.P.·Product code KWS·August 10, 2011
MOTORIZED 3-WHEELED VEHICLE FOR OUTSIDE TRANSPORT
FDA Adverse Event
C.T.M. HOMECARE PRODUCT, INC·Product code INI·July 12, 2013
ALINITY I HAVAB IGG REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LOL·November 26, 2025
ALINITY I HAVAB IGG REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LOL·July 22, 2025
ALINITY I HAVAB-IGG REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LOL·June 25, 2025
ALINITY I HAVAB-IGG REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LOL·June 25, 2025
ALINITY I HAVAB IGG REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LOL·January 23, 2026
ALINITY I HAVAB IGG REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LOL·January 16, 2026
T-Cell Xtend REF TTK.610 US
FDA Recall
Open, Classified
·OXFORD IMMUNOTEC LTD
143 Park Road
Abingdon United Kingdom·Product code OJN·July 7, 2022
T-SPOT.TB REF TB.300 US
FDA Recall
Open, Classified
·OXFORD IMMUNOTEC LTD
143 Park Road
Abingdon United Kingdom·Product code OJN·July 7, 2022
AIM-V Medium REF AV.200/500
FDA Recall
Open, Classified
·OXFORD IMMUNOTEC LTD
143 Park Road
Abingdon United Kingdom·Product code OJN·July 7, 2022