FDA applicant
Beavers Dental, Div. Sybron Canada, Ltd.
FDA records 3 decisions for Beavers Dental, Div. Sybron Canada, Ltd. (Washington, DC) from 1986 to 2012: 3 510(k) clearances. Most are in product codes DZP (Instrument, Diamond, Dental) and EJL (Bur, Dental). 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 Beavers Dental, Div. Sybron Canada, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2012
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Beavers Dental, Div. Sybron Canada, 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) Report