Autorizaciones FDA 510(k)
Dispositivos autorizados mediante 510(k) seguidos por MedTracker
INI
2026-08-10
OHS
2026-08-10
Eye Recovery Pro (PH-e03)
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OHT
2026-08-10
Hair Removal Device (R3C16-G Pro, R3C16-V Pro)
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PKL
2026-08-10
Hemoclip (511 series, 543 series)
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QIH
2026-08-10
Prostate Core
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HGM
2026-08-10
Novii+ Wireless Patch System
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MPA
2026-08-10
Nova Eye iTrack™ 250A Canaloplasty Microcatheter (iTrack™ 250A)
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FMI
2026-08-10
Pen Needle (Ordinary Type I, Safety Type IIA, Safety Type IIB, Safety Type IIIA, Safety Type IIIB, Safety Type IV, Safety Type V, Ordinary Type VIA, Ordinary Type VIB, Ordinary Type VIC, Safety Type VII, Ordinary Type IB, Safety type VIII, Safety Type IX, Safety Type X, Ordinary Type XI, Safety Type XII)
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INI
2026-08-10
Mobility Scooter (W3465, W3902 (S50 Carbon))
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MEH
2026-08-10
Icona Hip Stem
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FOZ
2026-08-10
Unimpregnated Central Venous Catheter
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FGB
2026-08-07
Zamenix™ P
Ver detalles →No hay dispositivos coincidentes.
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