13 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ClearLink Controlled Phototherapy Equipment
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Monoject
FDA UDI
Cardinal Health, Inc.·10884521544659·Hypodermic Safety Needle
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526550148·GENUMEDI PT KNEE SUP SILVER L EW V
Monoject
FDA UDI
Cardinal Health 200, LLC·10192253025033·Hypodermic Safety Needle 22G x 1.5 in.
(0.7 x 3...
SSW CARBIDE GREAT WHITE
FDA UDI
Ss White Burs, Inc.·D6901822152·GREAT WHITE GOLD CARBIDE GW1557 - 5 PACK
Vilex Power Accessory
FDA UDI
VILEX IN TENNESSEE, INC.·00841731122292·Kwire .070X9" (1.8x225mm)
KIRSCHNER WIRES, STEINMAN PINS
FDA 510(k)
FDA Class 2
·Orthopedic
OSTEORAPTOR SUTURE ANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
MONOJECT HYPODERMIC SAFETY NEEDLE 22G,1 1/2
FDA Adverse Event
Injury
·SOL-MILLENNIUM MEDICAL INC.·Product code FMI·March 8, 2021
TENDRIL DX
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC. CRMD·Product code DTB·January 13, 2014
GOBED II
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·June 21, 2013
OCTRODE 60-CM LENGTH PERCUTANEOUS LEAD
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 7, 2011
LEEP PRECISION GENERATOR
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code HGI·August 19, 2022