FDA applicant
Tulsa Dental Products, Ltd.
FDA records 8 decisions for Tulsa Dental Products, Ltd. (Tulsa, OK) from 1988 to 1997: 8 510(k) clearances. Most are in product codes EKM (Gutta-Percha) and DZA (Drill, Dental, Intraoral). Its devices cite 1 predicate, 1 of them its own earlier devices. 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 Tulsa Dental Products, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Tulsa Dental Products, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Tulsa Dental Products, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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