FDA applicant
Tti Medical
FDA records 9 decisions for Tti Medical (Pleasanton, CA) from 1987 to 1995: 9 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and GEI (Electrosurgical, Cutting & Coagulation &…). 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 Tti Medical’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Tti Medical since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Tti Medical’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