9 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LACTOSORB SUTURE ANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
LEVEL ONE
FDA UDI
KLS-Martin L.P.·00888118118424·
LEVEL ONE
FDA UDI
KLS-Martin L.P.·00888118118431·
PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
O'NEIL URINARY CATHETER INTRODUCER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ADAPTA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·February 11, 2013
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·July 24, 2014
ECHELON*FLEX60
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·January 10, 2011
Synthes Sciatic Nerve Retractor and Sciatic Nerve Retractor Long; Synthes Sciatic Nerve Retractor and Sciatic Nerve Retractor Long are system specific instruments to the 3.5 mm Low Profile Pelvic System Retractor Set.
FDA Enforcement
Class II
·Terminated·Synthes (USA) Products LLC·August 26, 2015