# Aesthetic Technology, Ltd.

- Location (FDA's records): Warrington, GB
- FDA decisions: 4 (2020–2024): 4 510(k) clearances
- Product codes: GEX (2), ILY (1), OHS (1)
- 510(k) review time since 2016: median 121 days, against 90 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 8 (2 its own); citations of its devices by later devices: 7 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Biophotas, Inc.: 2 (https://510kreport.com/company/biophotas)
- Trophy Skin, Inc.: 1 (https://510kreport.com/company/trophy-skin)
- Gtg Wellness Co., Ltd.: 1 (https://510kreport.com/company/gtg-wellness)
- Shanghai Apolo Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/shanghai-apolo-medical-technology)
- Ningbo Hesi Electric Co., Ltd.: 1 (https://510kreport.com/company/ningbo-hesi-electric)

## Firms that cite its devices most
- Emoled, Srl: 1 (https://510kreport.com/company/emoled)
- Inwound Aps: 1 (https://510kreport.com/company/inwound)
- Shenzhen Kaiyan Medical Equipment Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-kaiyan-medical-equipment)
- Shenzhen Hanhua Opto Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-hanhua-opto)
- Fit-Pro KFT (Ltd.) - DBA E-Fit: 1 (https://510kreport.com/company/fit-pro-kft-dba-e-fit)

## Its most-cited devices
- K200659: Dermalux Tri-Wave MD (2020), cited by 3
- K212275: Dermalux Flex MD (2021), cited by 3
- K202028: dermalux Flex MD (2020), cited by 1

## Recent decisions
- K240222: Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024) (Jun 4, 2024)
- K212275: Dermalux Flex MD (Nov 18, 2021)
- K202028: dermalux Flex MD (Dec 16, 2020)
- K200659: Dermalux Tri-Wave MD (May 9, 2020)

Source page: https://510kreport.com/company/aesthetic-technology