# K912734: Interpore Hex Head Implant Restorative Components

- Pathway: 510(k) (Traditional)
- Applicant: Interpore Intl.
- Decided: Jan 8, 1992 after 202 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.
350 later devices descend from it; 1 cites it directly.
0 of 351 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
- K962023: Plastic Protection Healing Caps (1996), 349 descendants of its own
- K051717: RN Synocta Temporary Meso Abutment (2005), 318 descendants of its own
- K070478: P.004 RC Temporary Abutment, P.004 Temporary Healing Abutment (Cap) (2007), 283 descendants of its own
- K072679: P.004 Abutments (2007), 279 descendants of its own
- K092814: Straumann Dental Abutments (2009), 223 descendants of its own

Source page: https://510kreport.com/device/K912734
Methodology: https://510kreport.com/methodology