# K953235: Screw Implants, Grade 3; Uncoated, HA, TP-K3

- Pathway: 510(k) (Traditional)
- Applicant: The Implant Center of the Palm Beaches
- Decided: Sep 13, 1995 after 64 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.
12 later devices descend from it; 1 cites it directly.
0 of 13 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
- K121406: Inclusive Tapered Implant System (2013), 11 descendants of its own
- K143353: Hahn Tapered Implant System (2015), 10 descendants of its own
- K170044: Inclusive Titanium Abutments compatible with: MegaGen AnyRidge Implant System (2017), 5 descendants of its own
- K191222: Inclusive Titanium Abutments compatible with: Dentsply Implants Astra Tech Implant System EV (2019), 4 descendants of its own
- K153099: Inclusive Tapered Implant System (2016), 3 descendants of its own

Source page: https://510kreport.com/device/K953235
Methodology: https://510kreport.com/methodology