10 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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TEAR VOLUME TESTS
FDA 510(k)
FDA Class 1
·Ophthalmic
Archon
FDA UDI
Nuvasive, Inc.·00887517311252·Archon Screw, 4.5x15mm S.T. Fixed
Avance® Solo
FDA UDI
Mölnlycke Health Care AB·07323190236008·Avance Solo Border Dressing 15x15 cm
Snowden-Pencer
FDA UDI
STERIS CORPORATION·10885403141102·Snowden-Pencer KLEINERT-KUTZ HOOK 3MM DIAMETER ...
MODEL LS-80 ADULT VENTILATION MONITOR
FDA 510(k)
FDA Class 2
·Anesthesiology
NEOMED DUAL LUMEN UMBILICAL CATHETER, MODELS S2UVC4.0, S2UVC5.0
FDA 510(k)
FDA Class 2
·General Hospital
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·June 18, 2014
ECHELON*FLEX60
FDA Adverse Event
Injury
·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code GDW·October 25, 2010
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON INC·Product code FTL·December 20, 2012
CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010, 17C1040, 17C2040
FDA Enforcement
Class II
·Completed·Townsend Design·January 17, 2024