29 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DAIG VESSEL DILATOR
FDA 510(k)
FDA Class 2
·Cardiovascular
Reprocessed 2.5mm Drill Bit
FDA UDI
SURETEK MEDICAL·B390AR8943301·
NA
FDA UDI
STERILMED, INC.·10888551012782·DRILL BIT
Arthrex
FDA UDI
Provision·B504OMAR8943300·
Arthrex®
FDA UDI
ARTHREX, INC.·00888867052376·2.5mm Drill Bit
Arthrex
FDA UDI
Provision·00810041061539·
ALBUMIN REAGENT FOR DEMAND ANALYZER
FDA 510(k)
FDA Class 2
·Clinical Chemistry
IS-2000 DIGITAL OPHTHALMIC IMAGING SYSTEM
FDA 510(k)
FDA Class 2
·Ophthalmic
Arthrex®
FDA UDI
ARTHREX, INC.·00888867265745·2.5MM DRILL BIT, REUSABLE
PLUM A+ DRIVER ED 2
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·April 23, 2014
BASX BLADELESS
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·November 9, 2010
OMNIPOD INSULIN PUMP
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code LZG·November 16, 2012
LO-PRO SCRW,TI,3.5MMX 14MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HWC·March 20, 2024
CORTICAL BONE SCREW, Ø3.5MM X 32MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code KTW·November 26, 2025
LO-PRO SCRW,TI,3.5MMX 16MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HWC·October 1, 2025
ALPHA PLATE, RIGHT, 18 HOLE
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HRS·November 26, 2025
LO-PRO SCRW,TI,3.0MMX 20MMCORT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·August 16, 2023
LO-PRO SCRW,TI,3.5MMX 12MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·August 17, 2023
3.0 X 14MM VAL SCREW, TI
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·August 17, 2023
3.0 X 16MM VAL SCREW, TI
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·August 17, 2023