54 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Powerpress Recovery Unit
FDA 510(k)
FDA Class 2
·Physical Medicine
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772777617·LUMBAMED BASIC DORSAL STAY WM SILVER IV
LEONE SPA
FDA UDI
LEONE SPA·08033707061007·BRACKETS 22 MOL
SprintRay Standard Denture Base - Original Meharry
FDA UDI
Sprintray, Inc.·00850039704253·SprintRay Standard Denture Base is a light-cura...
24M - Southwest Gas Corp
FDA UDI
Certified Safety Manufacturing, Inc.·00766588010441·24M - Southwest Gas Corp
SURGISIS STAPLE LINE REINFORCEMENT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MAGNA FORTIS OPHTHALMOSCOPE DIAGNOSTIC KIT
FDA 510(k)
FDA Class 2
·Ophthalmic
NOBELACTIVE TIULTRA NP 3.5X13MM
FDA Adverse Event
Injury
·NOBEL BIOCARE AB·Product code DZE·May 31, 2021
NOBELACTIVE TIULTRA NP 3.5X13MM
FDA Adverse Event
Injury
·NOBEL BIOCARE AB·Product code DZE·May 31, 2021
Trabecular Metal®
FDA UDI
Zimmer, Inc.·00889024118751·
Trabecular Metal®
FDA UDI
Zimmer, Inc.·00889024118768·
Trabecular Metal®
FDA UDI
Zimmer, Inc.·00889024118744·
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 29, 2025
PHYSIOMESH UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·April 22, 2021
PROCEED MESH
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·April 22, 2021
BD SMARTSITE¿ VENTED VIAL ACCESS DEVICE, 20 MM
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code LHI·February 1, 2022
ENDURANT II STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·August 3, 2021
LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM WITH RAPIDPORT
FDA Adverse Event
Malfunction
·ALLERGAN·Product code LTI·June 27, 2013
JUVEDERM ULTRA PLUS
FDA Adverse Event
Injury
·ALLERGAN·Product code LMH·August 5, 2011
I-STAT 6+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE INC.·Product code MMI·September 23, 2008