FDA applicant
Firstline, LLC
FDA records 1 decision for Firstline, LLC (Buellton, CA) in 2005: 1 510(k) clearance. All are in product code LZA (Polymer Patient Examination Glove). 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 Firstline, LLC’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Firstline, LLC since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Firstline, LLC’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