44 results
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22ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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RETIC CHEX LINEARITY
FDA 510(k)
FDA Class 2
·Hematology
TOSCA Open end interface cable 5V FS
FDA UDI
Radiometer Basel AG·05700693096230·TOSCA Open end interface cable 5V FS
Immunalysis
FDA UDI
IMMUNALYSIS CORP·00840937108918·Multi-Drug Calibrator 2
PedCAT
FDA UDI
CURVEBEAM, LLC·00863152000300·Cone Beam Computed Tomography diagnostic imagin...
RECLAIM
FDA UDI
DEPUY (IRELAND)·10603295543879·RECLAIM MONOBLOC REVISION HIP SYSTEM MONOBLOC ...
Mariner Outrigger
FDA UDI
Seaspine Orthopedics Corporation·10889981172671·Axial, Closed, 115mm
Golden Isles Pedicle Screw System
FDA UDI
Intelivation, LLC·G079C2530001150·Curved Anti-Rotation Ti Rod, 115mm
e-vive NMES System; 2XL/3XL, Right
FDA UDI
Motive Health, Inc.·00854816006899·e-vive NMES System; 2XL/3XL, Right
PedFlex Flexible Nailing System
FDA UDI
ORTHOPEDIATRICS CORP.·00841132119419·ø1.5mm Flexible IM Nail Cap (2 Each)
Golden Isles Pedicle Screw System
FDA UDI
Intelivation, LLC·G079C2520001150·Curved Ti Rod, 115mm
Taurus Pedicle Screw System
FDA UDI
SINTX Technologies, Inc.·M555500000115·Taurus Implant Caddy- Screws
BARCOMED 2MP2
FDA 510(k)
FDA Class 2
·Radiology
MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (38 CM), MODEL 3555-38; MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (60 CM),
FDA 510(k)
FDA Class 2
·Neurology
EQ-5000 EQUATOR CONVECTIVE WARMER
FDA Adverse Event
Injury
·SMITHS MEDICAL ASD, INC.·Product code DWJ·September 21, 2009
PedFlex Flexible Nailing System
FDA UDI
ORTHOPEDIATRICS CORP.·00840194418287·Ø1.5 MM FLEXIBLE IM NAIL CAP (2 EACH)
RS GLENOID PLATE EXT CAG +10MM CAGE PEG
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWS·July 17, 2023
EQUINOXE REVERSE 42MM HUMERAL LINER +2.5
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·August 7, 2023
MEGASUTURECUT NEEDLEDRIVER INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC.·Product code NAY·March 8, 2013
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·February 18, 2011
SYNCHROMED EL
FDA Adverse Event
Injury
·RICE CREEK MANUFACTURING·Product code LKK·February 19, 2008