# AZmed

- Location (FDA's records): Paris, FR
- FDA decisions: 6 (2022–2026): 6 510(k) clearances
- Names in FDA's records: AZmed (4); Azmed Sas (2)
- Product codes: QBS (4), QFM (1), MYN (1)
- 510(k) review time since 2016: median 102 days, against 123 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 6 (3 its own); citations of its devices by later devices: 3 (3 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
- Lunit, Inc.: 1 (https://510kreport.com/company/lunit)
- Samsung Electronics Co., Ltd.: 1 (https://510kreport.com/company/samsung-electronics)
- Imagen Technologies, Inc.: 1 (https://510kreport.com/company/imagen-technologies)

## Its most-cited devices
- K240845: Rayvolve (2024), cited by 1
- K220164: Rayvolve (2022), cited by 1
- K260378: Rayvolve (2026), cited by 1

## Recent decisions
- K261378: Rayvolve AZchest (Aug 28, 2026)
- K260378: Rayvolve (May 12, 2026)
- K243831: Rayvolve LN (Mar 26, 2025)
- K243808: Rayvolve PTX-PE (Mar 21, 2025)
- K240845: Rayvolve (Jul 17, 2024)
- K220164: Rayvolve (Jun 2, 2022)

Source page: https://510kreport.com/company/azmed