ClearanceBrief
Company ยท IT

M.D.L. S.r.l.

FDA 510(k) clearances and medical device recalls filed under this name, 2016 to 2016. Name variants (Inc, Corp, punctuation) are merged.

1510(k) clearances (0 in 12 months)
5recalls (0 in 12 months)
1recalls that name a 510(k)

Product codes

CodeDeviceRecords
KNWInstrument, Biopsy2
DWONeedle, Biopsy, Cardiovascular1
GAANeedle, Aspiration And Injection, Disposable1
GDFGuide, Needle, Surgical1
MJGDevice, Percutaneous, Biopsy1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 27, 2016K160316SemiCut Semi-automatic Biopsy Needle, Themy Automatic Disposable Biopsy Device, Palium Automatic Reusable Biopsy Device,
M.D.L. S.R.L., IT
KNW

Latest recalls

DateFirm and productCodeLinked 510(k)
Aug 5, 2021M.D.L. S.r.l.
General Manual surgical instrument
Terminated
MJGNone listed
Aug 5, 2021M.D.L. S.r.l.
Soft Tissue Biopsy Needles
Terminated
KNWK160316
Aug 5, 2021M.D.L. S.r.l.
Mammary Nodules Localization
Terminated
GDFNone listed
Aug 5, 2021M.D.L. S.r.l.
Aspirated Cyto-Histological Biopsy needle
Terminated
GAANone listed
Aug 5, 2021M.D.L. S.r.l.
Bone Marrow Transplantation biopsy needle
Terminated
DWONone listed
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