FDA applicant
Moor Instruments, Ltd.
FDA records 14 decisions for Moor Instruments, Ltd. (Axminster, Devon, GB) from 1991 to 2016: 14 510(k) clearances. Most are in product codes DPT (Probe, Blood-Flow, Extravascular) and GEX (Powered Laser Surgical Instrument). Its devices cite 15 predicates, 11 of them its own earlier devices. 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 Moor Instruments, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2016
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Moor Instruments, 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