33 results
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38ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VSI TORQUE DEVICE
FDA 510(k)
FDA Class 2
·Cardiovascular
PIVOT Extra Coarse Mint Prophy Pack Box 100
FDA UDI
Preventech·D0241100093·PIVOT Extra Coarse Mint Prophy Pack Box of 100 ...
OsteoMed
FDA UDI
OSTEOMED LLC·00845694001526·19mm Left L Plate, 1.0mm Thick
LEONE SPA
FDA UDI
LEONE SPA·08033707092926·BKT F1000 SELF LIGATING ROTH 22
MATHIEU NEEDLE HOLDER
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896045989·MATHIEU NEEDLE HOLDER DELICATE TUNGSTEN CARBIDE...
AngelMed Guardian Programmer External Power Accessories
FDA UDI
Avertix Medical Inc.·00850012625100·PROG-003 External Power Accessories Kit (US)
REMSTAR AUTO A-FLEX
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·January 29, 2025
NON-INVASIVE VENTILATION NIV OPTION, MODEL 84 14 474
FDA 510(k)
FDA Class 2
·Anesthesiology
PROFILE-V MEDTOXSCAN DRUGS OF ABUSE TEST SYSTEM AND 12 DRUGS TEST SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Widex
FDA UDI
Widex A/S·05706069423860·Widex T-DEX (complete) (DEX silver )
Widex
FDA UDI
Widex A/S·05706069445046·Widex FM+DEX (DEX silver )
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·October 6, 2025
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·October 6, 2025
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025
SMR GLENOSPHERE Ø 36MM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code KWS·September 20, 2022
REZUM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·March 13, 2026
INTELLICUFF
FDA Adverse Event
Malfunction
·HAMILTON MEDICAL AG·Product code BSK·January 8, 2025
INTELLICUFF
FDA Adverse Event
Malfunction
·HAMILTON MEDICAL AG·Product code BSK·January 8, 2025
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025