# Ya-Man, Ltd.

- Location (FDA's records): Tokyo, JP
- FDA decisions: 6 (2001–2025): 6 510(k) clearances
- Product codes: NFO (3), GEX (2), ILY (1)
- 510(k) review time since 2016: median 243 days, against 124 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 6 (2 its own); citations of its devices by later devices: 3 (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
- Leto Enterprise, Ltd.: 2 (https://510kreport.com/company/leto-enterprise)
- Usa Laser Biotech, Inc.: 1 (https://510kreport.com/company/usa-laser-biotech)
- Avicenna Laser Technology, Inc.: 1 (https://510kreport.com/company/avicenna-laser-technology)

## Firms that cite its devices most
- Guangdong Newdermo Biotech Co., Ltd.: 1 (https://510kreport.com/company/guangdong-newdermo-biotech)

## Its most-cited devices
- K220198: Medi Lift PLUS (2023), cited by 3

## Recent decisions
- K250618: Medi Lift Essential Eye Mask (Oct 29, 2025)
- K244048: Medi Lift Mask (Jan 16, 2025)
- K220198: Medi Lift PLUS (Jun 28, 2023)
- K112016: L-Ser KO Lamp (Feb 10, 2012)
- K032944: YA-Man Laser 21 (Dec 19, 2003)
- K011021: LASER 20 (Oct 9, 2001)

Source page: https://510kreport.com/company/ya-man