FDA applicant
Asset Medikal Tasarim Sanayi VE Ticaret A.S.
FDA records 1 decision for Asset Medikal Tasarim Sanayi VE Ticaret A.S. (Istanbul, TR) in 2024: 1 510(k) clearance. All are in product code LHI (Set, I.V. Fluid Transfer). 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 Asset Medikal Tasarim Sanayi VE Ticaret A.S.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2024
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2024.
Planning a device like Asset Medikal Tasarim Sanayi VE…’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) ReportOther applicant names beginning “Asset”
FDA records each applicant name separately; these may or may not be the same firm.