FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
GEI
2024-07-12
OLO
2024-07-12
TMINI Miniature Robotic System (TMINI 1.1)
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NDS
2024-07-12
MoFi Cell Culture Basal Medium
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NPM
2024-07-12
Geistlich Bio-Oss®
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HGX
2024-07-12
MilkMate Breast Pump (A0006); MilkMate Kit (sterile, single-use only), 21 mm breast shield (A0005-21); MilkMate Kit (sterile, single-use only), 24 mm breast shield (A0005-24)
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FAJ
2024-07-12
Endoscopic Video Image Processor (RP-IPD-V2000EF); Single-Use Video Flexible Cysto-Nephroscope (RP-U-C01F, RP-U-C01FS)
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GEI
2024-07-12
Megadyne Patient Return Electrode Pad - Universal Dual (model 0846), Megadyne Patient Return Electrode Pad - Universal Plus (model 0847), Megadyne Patient Return Electrode Pad - Universal Dual Plus (model 0848)
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JAK
2024-07-12
HiRise (1040-230)
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PKL
2024-07-12
Single Use Hemoclips
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HRS
2024-07-12
KLS Martin Orthopedic Implants - MR Conditional
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NHA
2024-07-12
Inclusive® Titanium Abutments compatible with: Keystone® Dental PrimaConnex®, Neodent® GM, Straumann® BLX, Implant Direct® Legacy®, Implant Direct® InterActive®, Implant Direct® RePlant® Implant Systems
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KCT
2024-07-12
S.I.N. Instrument Kits
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