# K101382: DPL Nuve

- Pathway: 510(k) (Traditional)
- Applicant: Led Technologies, LLC
- Decided: Nov 9, 2010 after 176 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
No predicates in its family tree.
45 later devices descend from it; 1 cites it directly.
0 of 46 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Omnilux New U: named in the summary without a submission number
- (no number) Tanda Skin Care product: named in the summary without a submission number

## Most influential descendants
- K141181: Nuve for Wrinkles, DPL Nuve for Wrinkles (2015), 44 descendants of its own
- K171390: dpl II Panel (2017), 28 descendants of its own
- K171386: dpl SpectraLite (2017), 19 descendants of its own
- K180320: dpl IIa Panel (2018), 14 descendants of its own
- K172909: Elevare, Perfectio 4 (2018), 11 descendants of its own

## Indications for use
Intended to emit energy in the red and infrared region of the spectrum for use in dermatology for the treatment of periorbital wrinkles. indicated as an over-the-counter phototherapy device for the treatment of mild to moderate acne.

Source page: https://510kreport.com/device/K101382
Methodology: https://510kreport.com/methodology