9 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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THE SWIRLER NEBULIZER
FDA 510(k)
FDA Class 2
·Anesthesiology
Laminoplasty
FDA UDI
Seaspine Orthopedics Corporation·10889981096038·4mm Mouth, Side by Side Implant Caddy
Ophthalmic Forceps
FDA UDI
KATENA PRODUCTS, INC.·00841668106396·GIRARD FORCEPS 0.12MM LEFT
POWER RIGHT ANGLE LINEAR CUTTER DIGITAL LOADING UNIT WITH RELOADS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Orca Air/Water and Suction Valves
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ATTAIN STARFIX
FDA Adverse Event
Injury
·MPRI·Product code OJX·February 9, 2013
COLLEAGUE CXE VOLUMETRICINFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·January 7, 2011
LINOX SMART S DX 65/17
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code NVY·July 23, 2014
BIOMET StageOne Hip Cement Spacer Mold with Insert, 56 MM, Silicone, Sterile, Item 431183.
FDA Enforcement
Class II
·Terminated·Biomet, Inc.·April 15, 2020