FDA applicant
Perspectum, Ltd.
FDA records 8 decisions for Perspectum, Ltd. (Oxford, GB) from 2020 to 2026: 8 510(k) clearances. Most are in product codes LNH (System, Nuclear Magnetic Resonance Imaging) and LLZ (System, Image Processing, Radiological). Since 2016 its 510(k)s took a median of 92 days from receipt to decision, against 124 for FDA’s reviews in the same codes and years. Its devices cite 12 predicates, 4 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Perspectum”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Perspectum, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2024
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2020.
Planning a device like Perspectum, 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) ReportOther applicant names beginning “Perspectum”
FDA records each applicant name separately; these may or may not be the same firm.