FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
LNH
2026-02-23
KNW
2026-02-23
ZeniCore™ Automatic Biopsy Instrument (863212100 / ZeniCore Automatic Biopsy Device 12ga x 10cm with Coaxial Introducer Kit); ZeniCore™ Automatic Biopsy Instrument (863212130 / ZeniCore Automatic Biopsy Device 12ga x 13cm with Coaxial Introducer Kit); ZeniCore™ Automatic Biopsy Instrument (863214100 / ZeniCore Automatic Biopsy Device 14ga x 10cm with Coaxial Introducer Kit); ZeniCore™ Automatic Biopsy Instrument (863214130 / ZeniCore Automatic Biopsy Device 14ga x 13cm with Coaxial
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FMF
2026-02-23
Profoject™ Insulin Syringes; Profoject™ Safelock Disposable Insulin Syringe
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NKB
2026-02-23
Duet™ Spinal Fixation System
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KGW
2026-02-23
Alexis® Lighted Wound Protector-Retractor, Rigid, Medium (CL402); Alexis® Lighted Wound Protector-Retractor, Flexible, Medium (CL302)
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KLE
2026-02-23
VITA VMLC Primer
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FDT
2026-02-22
Single Use Distal Cover MAJ-2315 (MAJ-2315)
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FDI
2026-02-21
Advanced Tissue Resection Device
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OWB
2026-02-20
CARA System
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MQL
2026-02-20
CaseBio™ Culture w/HSA (CMH5); CaseBio™ Handling w/HSA (WHH5)
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FMK
2026-02-20
Safety Heel Lancet
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OBP
2026-02-20
SPRY TMS Therapy System (0550)
View Details →No matching devices.
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