# K003090: Midmark Procenter Instrument Delivery System

- Pathway: 510(k) (Abbreviated)
- Applicant: Midmark Corp.
- Decided: Oct 18, 2000 after 15 days
- Product code: EIA (Unit, Operative Dental)
- Device class: 1
- Regulation: 21 CFR 872.6640
- 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; 1 cites 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K120239: Elevance (2012), 4 descendants of its own
- K143696: Spirit (2015), 2 descendants of its own
- K173608: Forest Dental Unit (2018), 1 descendant of its own
- K251626: Midmark Dental Delivery System (2025), 0 descendants of its own
- K231297: Firstar Dental Unit (2025), 0 descendants of its own

Source page: https://510kreport.com/device/K003090
Methodology: https://510kreport.com/methodology