FDA applicant
Creavo Medical Technologies, Ltd.
FDA records 1 decision for Creavo Medical Technologies, Ltd. (Coventry, GB) in 2017: 1 510(k) clearance. All are in product code DPS (Electrocardiograph). Its devices cite 1 predicate, 0 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 Creavo Medical Technologies, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2017
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2017.
Planning a device like Creavo Medical Technologies, 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