# K023336: Oco Dental Implant (5.0MM Diameter)

- Pathway: 510(k) (Special)
- Applicant: O Co., Inc.
- Decided: Oct 9, 2002 after 2 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.
5 later devices descend from it; 3 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K090174: Tsi; Eri (2009), 4 descendants of its own
- K110337: Universal Maxillary Molar (2012), 1 descendant of its own
- K171197: Zuga Dental Implant System (2018), 0 descendants of its own
- K142846: BBX1, BBX2, BBX1MO, BBX1MC (2016), 0 descendants of its own
- K122198: 6.00MM X 6.00MM Macro External Implant System (2013), 0 descendants of its own

## Indications for use
"0" Company's OCO Endosseous Implant is intended to be surgically placed in the bone of the upper or lower jaw arches providing support for prosthetic devices resulting in the restoration of the patient's chewing function,

Source page: https://510kreport.com/device/K023336
Methodology: https://510kreport.com/methodology