Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ItalyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list M.D.L. S.r.l. with 5 device recalls and 1 510(k) clearance. The most recent is a device recall dated Aug 5, 2021: Soft Tissue Biopsy Needles.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Aug 5, 2021 | Soft Tissue Biopsy NeedlesClass II · Sterility assurance may be compromised. | Device recalls |
| Aug 5, 2021 | Mammary Nodules LocalizationClass II · Sterility assurance may be compromised. | Device recalls |
| Aug 5, 2021 | General Manual surgical instrumentClass II · Sterility assurance may be compromised. | Device recalls |
| Aug 5, 2021 | Aspirated Cyto-Histological Biopsy needleClass II · Sterility assurance may be compromised. | Device recalls |
| Aug 5, 2021 | Bone Marrow Transplantation biopsy needleClass II · Sterility assurance may be compromised. | Device recalls |
| Oct 27, 2016 | SemiCut Semi-automatic Biopsy Needle, Themy Automatic Disposable Biopsy Device, Palium Automatic Reusable Biopsy Device, EasyCut Semi-automatic Biopsy Needle, MDL Biopsy and Coaxial Introducer NeedlesK160316 · KNW | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
