# K110735: Tanda Max Otc System

- Pathway: 510(k) (Traditional)
- Applicant: Pharos Life Corporation
- Decided: Aug 3, 2011 after 140 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.
84 later devices descend from it; 3 cite it directly.
0 of 85 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) Thinda Max System: named in the summary without a submission number
- (no number) Anti-wrinkle Light: named in the summary without a submission number

## Most influential descendants
- K141308: Nutra Light Red (2014), 81 descendants of its own
- K162098: LED Phototherapy Device (2017), 75 descendants of its own
- K171821: 2 Face / Face Evolution (2018), 58 descendants of its own
- K192295: PDT-Face (2020), 46 descendants of its own
- K212155: TheraFace LED (2021), 42 descendants of its own

## Indications for use
Thinda Max OTC is intended for the treatment of wrinkles, rhytides, and fine lines in the periorbital region.

Source page: https://510kreport.com/device/K110735
Methodology: https://510kreport.com/methodology