123 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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HI-TORQUE Steelcore Bare Guide Wire
FDA 510(k)
FDA Class 2
·Cardiovascular
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772777617·LUMBAMED BASIC DORSAL STAY WM SILVER IV
24M - Southwest Gas Corp
FDA UDI
Certified Safety Manufacturing, Inc.·00766588010441·24M - Southwest Gas Corp
GERALD TISSUE FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896060210·GERALD TISSUE FORCEPS TUNGSTEN CARBIDE PLATFORM...
Initia Total Hip System
FDA UDI
KYOCERA CORPORATION·04547898306785·MX LINER 32-52/54
Active Articulation Hip System
FDA UDI
Biomet Orthopedics, LLC·00880304485020·
3M™ Unitek™
FDA UDI
3M UNITEK CORPORATION·00652221047960·Ligature Wire 16 oz. Spool .014 Ea
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319742341·Noyes Alligator Forceps 5-1/2" (14cm) shaft, 1x...
DESS dental smart solutions
FDA UDI
TERRATS MEDICAL SL.·08435457201199·Conical BL
Active Articulation™ Dual Mobility Hip System
FDA UDI
Biomet Orthopedics, LLC·00880304491328·
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306805035·Tebbetts Ostetome, 3mm
SIEMENS INFINITY SC 6002XL MODIFICATIONS
FDA 510(k)
FDA Class 2
·Cardiovascular
NIPRO INSULIN SYRINGE
FDA 510(k)
FDA Class 2
·General Hospital
EZout
FDA UDI
STRYKER CORPORATION·07613327176094·Riser Ring, 44-46mm
ONE TOUCH ULTRA
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·March 11, 2005
ALINITY C PROCESSING MODULE
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code JJE·April 2, 2025
CAPSURE EPI
FDA Adverse Event
Death
·MEDTRONIC, INC.·Product code DTB·October 16, 2008
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 10, 2011
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·July 1, 2013
DELTA CER FEM HD 28/0MM T1
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·September 22, 2020