M.D.L. S.R.L.
M.D.L. S.R.L. holds FDA 510(k) medical device clearance, cleared in 2016, with 5 FDA device recalls on record.
Top product codes for M.D.L. S.R.L.
FDA recalls by M.D.L. S.R.L.
- Z-2493-2021 — General Manual surgical instrument
- Z-2492-2021 — Soft Tissue Biopsy Needles
- Z-2491-2021 — Mammary Nodules Localization
- Z-2490-2021 — Aspirated Cyto-Histological Biopsy needle
- Z-2489-2021 — Bone Marrow Transplantation biopsy needle
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by M.D.L. S.R.L.
Data sourced from openFDA. This site is unofficial and independent of the FDA.