FDA applicant
Lifelink Foundation Tissue Bank
FDA records 1 decision for Lifelink Foundation Tissue Bank (Tampa, FL) in 1992: 1 510(k) clearance. All are in product code LEM (Human Lyophilized Dura Mater). 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 Lifelink Foundation Tissue Bank’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Lifelink Foundation Tissue Bank since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Lifelink Foundation Tissue Bank’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) Report