FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
GEI
2026-07-13
HGX
2026-07-13
Wearable Breast Pump (Model S32A)
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SCR
2026-07-13
Hearing assist
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PFO
2026-07-10
Cochlear™ Osia® 3(I) Sound Processor;Cochlear™ Osia® 3 Sound Processor;Cochlear™ Osia® 3 Charger;Cochlear™ Osia® 3 Aqua+;Cochlear™ Osia® Fitting Software 3;Cochlear™ Osia® Smart App;Cochlear™ Osia® System
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ESW
2026-07-10
WallFlex Esophageal Stent System;Agile Esophageal Over-the-Wire (OTW) Stent System
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KNT
2026-07-10
Minnesota Four-Lumen Esophagogastric Tamponade Tube - 18 French (0092220); Blakemore Esophageal-Nasogastric Tube - 20 French (0092100); Blakemore Esophageal-Nasogastric Tube - 16 French (0092300)
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FOZ
2026-07-10
ClearSafe Closed System
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LLZ
2026-07-10
Avara Viewer
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LSR
2026-07-10
Sofia Lyme FIA; Sofia 2 Campylobacter FIA
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OWB
2026-07-10
SmartCT (R3.0 (L10))
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EOQ
2026-07-10
LungFlow Airway Catheter
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LPH
2026-07-10
Omnifit® 20° Series I Insert;Omnifit® Crossfire® 10° Series II Insert; Constrained Acetabular Insert; Trident® Crossfire® 0° Polyethylene Insert; Trident ® Crossfire ® 10° Polyethylene Insert;System 12 Crossfire® 10° Insert; Trident® 0° Constrained Acetabular Insert; Trident® Constrained Acetabular Liner;Trident® All Poly Constrained Acetabular Insert; Crossfire® Eccentric Insert 10°; Artisan® Bone Plug;UHR® Universal Head Bipolar Component
View Details →No matching devices.
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