Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
GYD
2026-08-20
OLO
2026-08-20
Remex Spine Surgery Navigation - Universal Instruments
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BTY
2026-08-20
CPETWise Platform
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SET
2026-08-19
Elecsys Phospho-Tau (217P) Plasma
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LNH
2026-08-19
Swoop® Portable MR Imaging® System
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SET
2026-08-19
PrecivityAD2 Test
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OWB
2026-08-19
EXTRON 3;EXTRON 6
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HRS
2026-08-19
Versalock Sterile Plating System
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DZE
2026-08-19
ZEROS Dental Implant System
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GEX
2026-08-19
ECHOLASER X4
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LXB
2026-08-19
Bone conduction Hearing Aid (BM100, BM300, BM310, SHOKZHEAR BM400, SHOKZ BM400MN, SHOKZHEAR BM410, SHOKZHEAR BM410MN, SHOKZHEAR BM420 and SHOKZHEAR BM420MN)
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GEX
2026-08-19
Diode Laser Therapy Systems (DL612A)
Ver detalhes →Nenhum dispositivo correspondente.
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