Aln S.A.R.L. is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Aln S.A.R.L. - FDA 510(k) Cleared Devices
Recent clearances: ALN Optional Vena Cava Filter (FB.010500, FF.010995, FJ.120096, FB.HOOK, FF.HOOK, FJ.HOOK)
1
Total
1
Cleared
0
Denied
Aln S.A.R.L. has 1 FDA 510(k) cleared medical devices. Based in Bormes Les Mimosas, FR.
Latest FDA clearance: Jun 2024. Active since 2024. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Aln S.A.R.L. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Aln S.A.R.L.
1 devices