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Moleculight, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K213840
MolecuLight I:X
May 18, 2022
K211901
MolecuLightDX
July 21, 2021
K210882
MolecuLight I:X
June 22, 2021
K191371
MolecuLight i:X
December 4, 2019
DEN180008
MolecuLight i:X
July 31, 2018