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/ Human Xtensions , Ltd.
Human Xtensions , Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K223718
HandX Self-Righting Needle Holder
June 5, 2023
K230491
HandX Monopolar Scissors
May 10, 2023
K222011
HandX Instrument - Monopolar Spatula
January 12, 2023
K212214
HandX
September 13, 2021
K203603
Monopolar Hook
February 1, 2021