26 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Arthrex VaultLock Glenoid
FDA 510(k)
FDA Class 2
·Orthopedic
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690110118·Femoral inserter
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916141783·ZEUS®-L Cup Curette Bayonet Angled Tip 8mm
Sentry
FDA UDI
Life Spine, Inc.·00190837034238·Ø5.5mm Tap
Scorpio
FDA UDI
Howmedica Osteonics Corp.·07613154020713·Cruciate Retaining Tibial Insert
STRYKER AUTO IRRIGATION SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
ERBE ESU MODEL VIO 100 C WITH ACCESSORIES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009116·INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009161·INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009154·INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009123·INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009147·INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009130·INTERMITTENT SUCTION REGULATORS
ASKU
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·January 3, 2026
ASKU
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·January 3, 2026
CLEARLINK CONTINU-FLO SOLUTION SET
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·December 6, 2021
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013
VENTED AUTOFEED HUMIDIFICATION CHAMBER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·July 13, 2011
FLO-GARD 6301 VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE (SG)·Product code FRN·September 17, 2008
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·December 29, 2016