FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
FGB
2025-02-11
QQX
2025-02-11
cobas® SARS-CoV-2 Qualitative for use on the cobas® 5800/6800/8800 Systems
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IYN
2025-02-11
Vivid iq
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BTR
2025-02-11
Rusch Endotracheal Tubes (Reinforced); Rusch Endotracheal Tubes (Safety Clear); Rusch Endotracheal Tubes (Safety Clear Pediatric)
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DZE
2025-02-11
LONGY Implant and LONGY-N Implant
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KCT
2025-02-11
NUVENTUS NV.C Surgical Cassette and Tray
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GEI
2025-02-11
InbellaBody System
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IYN
2025-02-11
Vivid T9/Vivid T8
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MQC
2025-02-10
Remi Custom Night Guard
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JWY
2025-02-10
The Sensititre 20-24 hour Haemophilus influenzae/Streptococcus pneumoniae (HP) MIC or Breakpoint Susceptibility System with penicillin in the dilution range of 0.015-32 ug/mL
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HRS
2025-02-10
Locking Plates and Screws Systems
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OHT
2025-02-10
Philips Lumea IPL
View Details →No matching devices.
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