FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
LLZ
2024-11-18
GEX
2024-11-18
Diode laser Treatment System (K18)
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ITI
2024-11-18
Power wheelchair
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ITI
2024-11-18
Power Wheelchair (W5538)
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DZE
2024-11-15
NUVENTUS NV.C Dental Implant System
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QRL
2024-11-15
Lancet (IA, IB, IC, ID, IE, IK, IL, IM, IIA, IIB, III, V, VI, VII, VIII, IX); Lancing device (HH-X-T, HH-XV-T, HH-XVI-T, HH-XVII-T, HH-XVIII-T, HH-XIX, HH-XXI-T, HH-XXII-T, HH-XXIII-T, HH-XXIV-T, HH-XXV-T, HH-XXVI-T, HH-XXVIII-T, HH-XXIX-T, HH-XXX-T, HH-XIII-T, HH-XXVII-T)
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OTM
2024-11-15
AdVance XP Male Sling System (720163-03)
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NLH
2024-11-15
Medline ReNewal Reprocessed Biosense Webster Webster CS Catheter with EZ Steer Technology and Medline ReNewal Reprocessed Biosense Webster Webster CS Catheter with EZ Steer Technology and Auto ID Technology (BD710DF282CT, BD710DF282RTS, BD710FJ282RTS, BD710FJ282CT)
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QFM
2024-11-15
VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage
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QOF
2024-11-15
Panther Fusion SARS-CoV-2/Flu A/B/RSV assay
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MQE
2024-11-15
VitaVitro® Single Lumen Oocyte Retrieval Needle (ORNS-17G, ORNS-18G), VitaVitro® Double Lumen Oocyte Retrieval Needle (ORND-17G)
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POK
2024-11-15
Koios DS
View Details →No matching devices.
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