25 results
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29ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SPECTRA-SYSTEM ABUTMENTS 2008
FDA 510(k)
FDA Class 2
·Dental
PureLife Dental
FDA UDI
PURELIFE, LLC·D79010811011·White "B" Ritter Tray Covers, 8 1/2" x 12 1/4",...
Armstrong
FDA UDI
MEDTRONIC XOMED, INC.·00613994146069·VENT TUBE 1081101 5PK ARMS MOD GROM 1.14
Microgel®
FDA UDI
MEDTRONIC XOMED, INC.·00763000037437·VENT TUBE 1081101 5PK ARMS MOD GROM 1.14
General Instrument
FDA UDI
ALPHATEC SPINE, INC.·00840180504871·Bone Funnel W/ Loading Trough
Caplugs/Evergreen
FDA UDI
CAPlugs·00810044202106·15 mL / 7.5 mL Prefilled Histoware Vials with Caps
Zimmer
FDA UDI
TEDAN SURGICAL INNOVATIONS, L.L.C.·00843059118896·Viewline Lateral Instrument Set Tray #1
n/a
FDA UDI
Ortho Development Corporation·00822409066476·Stem Extension Trial Diameter 8x110mm
NEEDLE 25X1-1/2 RB
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·January 31, 2025
XLTEK EVOKED POTENTIAL HEADBOX, MODEL EP-4
FDA 510(k)
FDA Class 2
·Neurology
RAICHEM ASSAYED CONTROL SERUM LEVEL 1 & 2
FDA 510(k)
FDA Class 1
·Clinical Chemistry
NEEDLE 25X1-1/2 RB
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·February 21, 2025
Optimotion Blue CR HCCR Total Knee System
FDA UDI
OPTIMOTION IMPLANTS LLC·B6961014P0811010·CR Tibial Insert, UHMWPE + Vitamin E, Size 8, ...
NEEDLE 25X1-1/2 RB
FDA Adverse Event
Injury
·BECTON DICKINSON·Product code FMI·January 31, 2025
WAVEWRITER ALPHA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 24, 2023
SIG PS CEM FEM W/LUGS RT SZ3
FDA Adverse Event
Injury
·DEPUY-RAYNHAM,A DIV. OF DEPUY ORTHOPAEDICS 1219655·Product code NJL·April 26, 2013
CRYSTALENS ACCOMMDATING IOL
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code NAA·August 29, 2014
GREENLIGHT ADDSTAT
FDA Adverse Event
Malfunction
·AMS, INNOVATION CTR - SILICON VALLEY·Product code GEX·April 14, 2011
PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code KRO·October 15, 2025
BD PYXIS ANESTHESIA STATION ES SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION 303, INC.·Product code BRY·January 22, 2024