# K963066: Mentor Injection Port Detector (Ipd)

- Pathway: 510(k) (Traditional)
- Applicant: Mentor Corp.
- Decided: Sep 27, 1996 after 51 days
- Product code: LCJ (Tissue Expander And Accessories)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K905484 (1991). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K905484: Accu-Tec System for Tissue Expander Injection Port, Mentor Corp. (1991) Summary page 4.

## Most influential descendants
- K221127: Sientra, inc. Portfinder (2023), 0 descendants of its own

## Indications for use
The Mentor Injection Port Detector is used to locate Mentor Tissue Expander remote and integral injection ports. The device is nonsterile and for postoperative use only.

Source page: https://510kreport.com/device/K963066
Methodology: https://510kreport.com/methodology