# K010343: BMR Dental Implant System, Model 3.3XX, Either HA or TPS Coated, 3.308, 3.310,3.312, 3.314 3.316

- Pathway: 510(k) (Traditional)
- Applicant: Buck Medical Research
- Decided: Feb 14, 2001 after 9 days
- Product code: DZE (Implant, Endosseous, Root-Form)
- Device class: 2
- Regulation: 21 CFR 872.3640
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K031322: Intra-Lock Hydroxyapatite Coated Implants (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K010343
Methodology: https://510kreport.com/methodology