FDA applicant
Davis Schottlander & Davis, Ltd.
FDA records 7 decisions for Davis Schottlander & Davis, Ltd. (Tonawanda, NY) from 1996 to 2004: 7 510(k) clearances. Most are in product codes ELM (Denture, Plastic, Teeth) and EIH (Powder, Porcelain). 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 Davis Schottlander & Davis, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Davis Schottlander & Davis, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Davis Schottlander & Davis, Ltd.’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) ReportOther applicant names beginning “Davis”
FDA records each applicant name separately; these may or may not be the same firm.