10 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INSTANT WARM GEL PACK
FDA 510(k)
FDA Class 1
·Physical Medicine
REVELATION DIAMOND
FDA UDI
Ss White Burs, Inc.·D6909127152·REVELATION DIAMOND 855-012C - 5 PACK
Gen. Acces/ Instr. Tip Guard
FDA UDI
KATENA PRODUCTS, INC.·00841668110850·TIP GUARDS VENTED WHITE PACK OF 100
HYGIA HEALTH SERVICES REPROCESSED NELLCOT D-25 OXISENSOR II
FDA 510(k)
FDA Class 2
·Cardiovascular
CANDELA GENTLEMAX FAMILY OF LASERS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SYMBIQ SINGLE CHANNEL
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·May 14, 2014
ON-Q PAIN PUMP
FDA Adverse Event
Injury
·I-FLOW, LLC·Product code MEB·January 8, 2013
UMBILI-CATH
FDA Adverse Event
Malfunction
·UTAH MEDICAL PRODUCTS, INC.·Product code FOS·November 17, 2010
PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code HSX·October 15, 2025
GENESIS UNI KNEE FEMORAL COMPONENT COCR
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code HSX·May 23, 2025