Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
BTT
2026-01-14
ODP
2026-01-14
Cervical Interbody and VBR Fusion System
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LZC
2026-01-14
Cardinal Health Nitrile Examination Gloves Extended Cuff
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OXO
2026-01-14
Orthoscan TAU MVP Mini C-Arm System
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MOS
2026-01-14
dS Base 1.5T; dS Base 3.0T; dS Head 1.5T; dS Head 3.0T; dS HeadNeck 1.5T; dS HeadNeck 3.0T
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KRD
2026-01-14
Concerto Versa™ Detachable Coil
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QNI
2026-01-13
BEAR® (Bridge-Enhanced ACL Restoration) Implant
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GCJ
2026-01-13
Connected OR Hub with Device and Voice Control; SDC4K Information Management System with Device and Voice Control
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KPS
2026-01-13
VERITON CT 300 Series Digital SPECT/CT System (VERITON CT 316/364); VERITON CT 400 Series Digital SPECT/CT System (VERITON CT 416/464)
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NKB
2026-01-13
Swedge™ Pedicle Screw Fixation System Bezier Rod
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LZA
2026-01-13
Non-sterile Powder Free Nitrile Examination Glove, Dual Color (White-Green), Tested for Use with Chemotherapy Drugs, Fentanyl Citrate, Xylazine HCl, and Simulated Gastric Acid; Non-sterile Powder Free Nitrile Examination Glove, Dual Color (White-Blue), Tested for Use with Chemotherapy Drugs, Fentanyl Citrate, Xylazine HCl, and Simulated Gastric Acid
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EJK
2026-01-13
Bright Cavity Liner
Ver detalhes →Nenhum dispositivo correspondente.
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