# LMH: Implant, Dermal, For Aesthetic Use

- Device class: 3; regulation: 21 CFR —; FDA's rule: PMA required
- FDA decisions: 22
- Recalls: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 2017: 52
- 2018: 57
- 2019: 68
- 2020: 61
- 2021: 51
- 2022: 40
- 2023: 81
- 2024: 74
- 2025: 51
- 2026: 56

## Most-cited predicates

Source page: https://510kreport.com/product-code/LMH
Data by year (CSV): https://510kreport.com/product-code/LMH.csv