Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
HIH
2025-12-18
QIH
2025-12-18
MediAI-BA
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HRS
2025-12-17
BRUSIO Trauma Toolbox System; TAMINA 3.5mm Proximal Humerus System
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QJU
2025-12-17
UltraSight Guidance
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HEB
2025-12-17
Unscented Menstrual Long Applicator Tampon; Unscented Menstrual Cardboard Applicator Tampon; Unscented Menstrual Digital Tampons
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OHS
2025-12-17
Wrinkle Retreat Pro Light Therapy Face Mask (Model: PH-m03)
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FMF
2025-12-17
DuoprossTM Smart Cap (Type I)
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FOZ
2025-12-17
SURFLO Hybria Closed System Safety IV Catheter
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NKB
2025-12-17
Vital™ Spinal Fixation System
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QBJ
2025-12-17
Dexcom G7 Continuous Glucose Monitoring (CGM) System, Dexcom G7 15 Day Continuous Glucose Monitoring (CGM) System
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DYB
2025-12-17
Intri26 Introducer Sheath
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QVP
2025-12-17
Elecsys Anti-SARS-CoV-2
Ver detalhes →Nenhum dispositivo correspondente.
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