# K960868: B.a.S.I.C. Dental Implant System

- Pathway: 510(k) (Traditional)
- Applicant: Danlin Products, Inc.
- Decided: Nov 14, 1996 after 255 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.
4 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K013682: Modification to Basic Dental Implant System (2001), 2 descendants of its own
- K072595: Omni-Tight (2008), 1 descendant of its own
- K082749: Omni-Tight (2008), 0 descendants of its own
- K022912: Post and Core - Thin for the Basic Dental Implant System (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K960868
Methodology: https://510kreport.com/methodology