FDA applicant
Michelson Diagnostics, Ltd.
FDA records 2 decisions for Michelson Diagnostics, Ltd. (Maidstone, GB) from 2010 to 2016: 2 510(k) clearances. All are in product code NQQ (System, Imaging, Optical Coherence Tomography…). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Michelson Diagnostics, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2016
2010high 1 (2010) · low 0 (2011)2026
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2010.
Planning a device like Michelson Diagnostics, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report