FDA applicant
3D Lifeprints UK, Ltd.
FDA records 2 decisions for 3D Lifeprints UK, Ltd. (West Derby, Liverpool, Merseyside, GB) from 2022 to 2023: 2 510(k) clearances. Most are in product codes PBF (Orthopaedic Surgical Planning And Instrument…) and DZJ (Driver, Wire, And Bone Drill, Manual). Its devices cite 2 predicates, 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 3D Lifeprints UK, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2023
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2022.
Planning a device like 3D Lifeprints UK, 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