FDA applicant
Artiberia
FDA records 79 decisions for Artiberia (San Antonio, TX) in 1985: 79 510(k) clearances. Most are in product codes GEN (Forceps, General & Plastic Surgery) and EMG (Forceps, Tooth Extractor, Surgical). 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 Artiberia’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Artiberia since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Artiberia’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