Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
CBI
2026-03-20
OZT
2026-03-20
Valvuloplasty Balloon Catheter (ValvuloPro)
Ver detalhes →
KGN
2026-03-19
Derma-Gide
Ver detalhes →
LPL
2026-03-19
Saview SH Optic 38 UV (Senofilcon A) Visibility Tinted Soft (Hydrophilic) Contact Lens; Saview SH Optic 38 UV toric (Senofilcon A) Visibility Tinted Soft (Hydrophilic) Contact Lens; Saview SH Optic 38 UV multifocal (Senofilcon A) Visibility Tinted Soft (Hydrophilic) Contact Lens
Ver detalhes →
DQX
2026-03-19
Enroute 0.014'' Transcarotid Guidewire
Ver detalhes →
FBN
2026-03-19
Disposable Distal Cap
Ver detalhes →
MRW
2026-03-19
DiversiVy™ Facet Screw System
Ver detalhes →
QKB
2026-03-19
AutoContour (RADAC V5)
Ver detalhes →
HRS
2026-03-19
CastleLoc Pectus Bar System
Ver detalhes →
KDI
2026-03-19
ELISIO™-H
Ver detalhes →
ILY
2026-03-19
CureLight Medical Diode Laser Systems (CureLight F2-A15; CureLight F2-B15; CureLight F2-A30; CureLight F2-B30; CureLight F3-AB30; CureLight F3-AB60.)
Ver detalhes →
ELW
2026-03-19
Dia-X Sil Bite
Ver detalhes →Nenhum dispositivo correspondente.
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