Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
INI
2026-08-10
OHS
2026-08-10
Eye Recovery Pro (PH-e03)
Ver detalhes →
OHT
2026-08-10
Hair Removal Device (R3C16-G Pro, R3C16-V Pro)
Ver detalhes →
PKL
2026-08-10
Hemoclip (511 series, 543 series)
Ver detalhes →
QIH
2026-08-10
Núcleo de Próstata
Ver detalhes →
HGM
2026-08-10
Novii+ Wireless Patch System
Ver detalhes →
MPA
2026-08-10
Nova Eye iTrack™ 250A Canaloplasty Microcatheter (iTrack™ 250A)
Ver detalhes →
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)
Ver detalhes →
INI
2026-08-10
Mobility Scooter (W3465, W3902 (S50 Carbon))
Ver detalhes →
MEH
2026-08-10
Icona Hip Stem
Ver detalhes →
FOZ
2026-08-10
Unimpregnated Central Venous Catheter
Ver detalhes →
FGB
2026-08-07
Zamenix™ P
Ver detalhes →Nenhum dispositivo correspondente.
Página 40 de 2763