# Levo AG

- Location (FDA's records): 5610 Wohlen, CH
- FDA decisions: 4 (2003–2015): 4 510(k) clearances
- Product codes: IPL (3), ITI (1)
- Predicates its devices cite: 7 (2 its own); citations of its devices by later devices: 8 (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
- Permobil AB: 2 (https://510kreport.com/company/permobil)
- Levo USA: 2 (https://510kreport.com/company/levo-usa)
- Sunrise Medical, Inc.: 1 (https://510kreport.com/company/sunrise-medical)

## Firms that cite its devices most
- Sunrise Medical (Us), LLC: 1 (https://510kreport.com/company/sunrise-medical-us)
- Upnride Robotics, Ltd.: 1 (https://510kreport.com/company/upnride-robotics)
- Etac Sverige AB: 1 (https://510kreport.com/company/etac-sverige)
- Parabasetec, GmbH: 1 (https://510kreport.com/company/parabasetec)
- E-Teng Technology, Inc.: 1 (https://510kreport.com/company/e-teng-technology)
- Motion Concepts: 1 (https://510kreport.com/company/motion-concepts)

## Its most-cited devices
- K051387: Levo Comfort II (2005), cited by 4
- K083017: LEVO C3 (2008), cited by 2
- K030893: Levo Combi (2003), cited by 2

## Recent decisions
- K140706: Levo Max (Jan 21, 2015)
- K083017: LEVO C3 (Oct 24, 2008)
- K051387: Levo Comfort II (Jun 10, 2005)
- K030893: Levo Combi (Apr 2, 2003)

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