ClearanceBrief
Company ยท CA

MolecuLight, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2018 to 2022. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
QJFAutofluorescence Imaging Adjunct Tool For Wounds4
QCRWound Autofluorescence Imaging Device1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 18, 2022K213840MolecuLight I:X
MolecuLight, Inc., CA
QJF
Jul 21, 2021K211901MolecuLightDX
MolecuLight, Inc., CA
QJF
Jun 22, 2021K210882MolecuLight I:X
MolecuLight, Inc., CA
QJF
Dec 4, 2019K191371MolecuLight i:X
MolecuLight, Inc., CA
QJF
Jul 31, 2018DEN180008MolecuLight i:X
MolecuLight, Inc., CA
QCR

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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