52 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STRATIFY JCV DXSELECT
FDA 510(k)
FDA Class 2
·Microbiology
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319704240·Littauer Cilia Forceps 3-1/2" (8.8cm), oblique,...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·10884450334833·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450313091·
SECA CORP.
FDA registration
SECA CORP.·4 products·🇺🇸 United States
MASTERGRAFT RESORBABLE CERAMIC
FDA 510(k)
FDA Class 2
·Orthopedic
CALLOS BONE VOID FILLER, SKAFFOLD NEXT GENERATION BONE VOID FILLER, OSTEO VATION
FDA 510(k)
FDA Class 2
·Orthopedic
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 21, 2024
VENTED HUMIDIFICATION CHAMBER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·May 20, 2013
ECHELON* 60 ENDOPATH**
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 13, 2011
ASCENSIA CONTOUR TS
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE, LLC·Product code NBW·August 13, 2008
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
TM ANKLE PROLONG TIBIAL INSERT SZ 6 +2
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HSN·August 14, 2018
TM ANKLE TIBIAL INSERT COMPONENT SIZE 4
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code ITW·August 9, 2018
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORP.·Product code OKS·August 19, 2014
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·January 13, 2017
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016