Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
HSB
2026-03-05
NHA
2026-03-04
Healing Abutment System
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KWQ
2026-03-04
ANTERIS Thoracolumbar Plate System
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KNW
2026-03-04
Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Control Module; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Disposable Probe, 8 gauge; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Disposable Targeting Set, 8 gauge; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Foot Switch; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Reusable Tray; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Battery Char
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MBI
2026-03-04
Aevumed FENIX Suture Anchor
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PBQ
2026-03-04
Mendit
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IYO
2026-03-04
QT Scanner 2000 Model A
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ITI
2026-03-04
Electric Wheelchair (MP148)
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PNN
2026-03-04
SureSmile Software
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DZE
2026-03-04
Dentis SQ-SL AXEL Fixture
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FTC
2026-03-04
Klär Lite (RCW-KL1000)
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NUH
2026-03-04
TENS/EMS device (GUSE01)
Ver detalhes →Nenhum dispositivo correspondente.
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