Autorizaciones FDA 510(k)
Dispositivos autorizados mediante 510(k) seguidos por MedTracker
DWF
2026-03-11
FRO
2026-03-11
LUOFUCON® Antimicrobial Wound Gel
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GEX
2026-03-11
Picasso Pro Diode Laser (002-00460)
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PHX
2026-03-11
INHANCE™ Reverse Shoulder System
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MBI
2026-03-11
Strut Suture; No-Tie Button
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IYN
2026-03-10
Sonosite iLOOK Ultrasound System
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OWB
2026-03-10
Alphenix, INFX-8000V/B, INFX-8000V/S, V9.6 with aEvolve Imaging (FOV Extension)
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NVK
2026-03-10
Gemini NOVA 810+980 Soft Tissue Laser
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HSB
2026-03-10
Reselute Tibial Nail
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N/D
2026-03-10
DePuy Synthes VOLT™ Medial Distal Femur 3.5 Plating System
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DZE
2026-03-10
Straumann® BLC Implants - Indication Widening
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EIH
2026-03-10
IPS e.max Zirconia
Ver detalles →No hay dispositivos coincidentes.
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