# K171386: dpl SpectraLite

- Pathway: 510(k) (Traditional)
- Applicant: Led Technologies, Inc.
- Decided: Aug 7, 2017 after 88 days
- Product code: OHS (Light Based Over The Counter Wrinkle Reduction)
- Device class: 2
- Regulation: 21 CFR 878.4810
- 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 K101190 (2010). 5 ancestors in all.
19 later devices descend from it; 3 cite it directly.
0 of 25 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141181: Nuve for Wrinkles, DPL Nuve for Wrinkles, Led Technologies, LLC (2015) Summary page 5.

## Most influential descendants
- K183247: dpl Faceware (2019), 10 descendants of its own
- K230042: Q-Rejuvalight Pro Facewear (Model: P19-0023) (2023), 9 descendants of its own
- K172662: reVive Perioral (2018), 4 descendants of its own
- K221444: LED Eye Perfector, model: EY-36A, EY-36B (2022), 3 descendants of its own
- K251588: LED Light Therapy Mask (FCM902, FCM905, FCM906, FCM908, 11-001-RBMASK, FCM910) (2025), 2 descendants of its own

## Indications for use
The dpl® SpectraLite is an Over-the-Counter (OTC) device intended for use in treating wrinkles within periorbital region.

Source page: https://510kreport.com/device/K171386
Methodology: https://510kreport.com/methodology