# K231852: BinkieRT

- Pathway: 510(k) (Traditional)
- Applicant: Papricalab
- Decided: Nov 15, 2023 after 145 days
- Product code: IYE (Accelerator, Linear, Medical)
- Device class: 2
- Regulation: 21 CFR 892.5050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K934523 (1995). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K183374: GrayDuck Stent, Poll Medical, LLC (2019) Summary page 5.

## Indications for use
The BinkieRT is intended to be used for repeat positioning and immobilization of a patient’s tongue and jaw while undergoing or receiving a course of external beam radiation therapy for treatment of cancer and other diseases. It is intended to be used by or under the direction of a licensed physician. BinkieRT is meant for use with 6 MV photon beams only.

Source page: https://510kreport.com/device/K231852
Methodology: https://510kreport.com/methodology