Aln S.A.R.L.
FranceFDA applicant, unverified FDA FEI 3007080617
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Aln S.A.R.L. makes
Aln S.A.R.L. manufactures optional vena cava filters, including retrievable and hook-equipped variants designed for venous thromboembolism prevention. These devices are intended for placement in the inferior vena cava to capture and retain thrombi, reducing the risk of pulmonary embolism. The portfolio includes both fixed and adjustable configurations to accommodate different clinical needs.
The company’s vena cava filters are classified as Class II medical devices under FDA regulations and are authorised through the 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) database, adhering to U.S. regulatory standards for venous filtration systems. The manufacturer operates from the United States.
Catalogue
ALN Optional Vena Cava Filter (FB.010500, FF.010995, FJ.120096, FB.HOOK, FF.HOOK, FJ.HOOK) Ref K241507
Regimes: CE MDR 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3007080617
- Address
- 589 CHEMIN DU NIEL, BORMES LES MIMOSAS Var
Frequently asked questions
How many devices does Aln S.A.R.L. have in the registry?
The registry currently lists 1 device for Aln S.A.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aln S.A.R.L.'s devices?
Among its 1 most recently registered device, Aln S.A.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Aln S.A.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aln S.A.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aln S.A.R.L. in the registry?
The most recently registered devices listed for Aln S.A.R.L. include ALN Optional Vena Cava Filter (FB.010500, FF.010995, FJ.120096, FB.HOOK, FF.HOOK, FJ.HOOK).