FDA applicant
Jay H. Geller
FDA records 4 decisions for Jay H. Geller (Santa Monica, CA) from 1994 to 1997: 4 510(k) clearances. Most are in product codes DZC (Wire, Orthodontic) and GGP (Test, Qualitative And Quantitative Factor…). 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 Jay H. Geller’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Jay H. Geller since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Jay H. Geller’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