# K232657: InnerView LC

- Pathway: 510(k) (Traditional)
- Applicant: Perimetrics, Inc.
- Decided: Sep 1, 2023 after 1 day
- Product code: EKX (Handpiece, Direct Drive, Ac-Powered)
- Device class: 1
- Regulation: 21 CFR 872.4200
- 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 K072213 (2008). 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)
- K072213: Perimetrics Periometer, Perimetrics, Inc. (2008) Summary page 4.

## Most influential descendants
- K251597: InnerView System (2025), 0 descendants of its own

## Indications for use
The InnerView LC is intended to precisely measure the damping characteristic of the periodontium and its associated fixed structures (teeth and/or implants). It can provide data to quantify tooth and/or dental implant mobility.

Source page: https://510kreport.com/device/K232657
Methodology: https://510kreport.com/methodology