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Levo AG

Active in EUDAMED

Switzerlandfrom SRN EUDAMED FDA SRN CH-MF-000008751 FEI 1000268398

Devices
12
Registrations
EUDAMEDFDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI
Authorised rep.
be-on-market GmbHDE

Catalogue12

  • C3 Ref LEVO C3/48

    Class I EUDAMED Active

  • Lcev Ref LCEV/L-XL/42/51

    Class I EUDAMEDFDA UDI Active

  • Levo Max Ref K140706

    Class II FDA 510(k) Active

  • Levo Comfort Ii Ref K051387

    Class II FDA 510(k) Active

  • Levo C3 Ref K083017

    Class II FDA 510(k) Active

  • Levo Combi Ref K030893

    Class II FDA 510(k) Active

  • Summit EL Ref SUMMIT EL/M/42/52

    Class I EUDAMED Active

  • Lcev Ref KID/XS/35/33

    Class I EUDAMED Active

  • Summit MA Ref SUMMIT MA/L/42/52

    Class I EUDAMED Active

  • Lcev Ref JR/XS/35/40

    Class I EUDAMED Active

  • Lae Ref LAE/S-M/48/57

    Class I EUDAMED Active

  • LCM2 Ref LCM2

    Class I EUDAMED Active

Company details

EUDAMED SRN
CH-MF-000008751
FDA FEI number
1000268398
EUDAMED status
Active
EUDAMED registered name
LEVO AG
EUDAMED abbreviated name
LEVO
Registered address
20, Anglikerstrasse, 5610, Wohlen, Switzerland
Website
www.levo.ch
Phone
+41566184411
PRRC contact
Branimir Borota(public in EUDAMED)

What Levo AG makes

Levo AG manufactures a range of manual and powered wheelchairs, including lightweight models (e.g., LCEV), mid-weight options (e.g., LEVO MAX, LEVO COMFORT II), and customisable configurations (e.g., LEVO COMBI, LEVO C3). Their portfolio also includes electric wheelchairs (e.g., Summit EL, Summit MA) and mobility aids such as leg elevators (LAE) and manual seating systems (LCM2).

The company’s devices are classified under EU Medical Device Regulation (MDR) as Class I or Class II, with corresponding listings in the EUDAMED registry. In the U.S., these products are documented via FDA 510(k) clearances. Levo AG is headquartered in Switzerland.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Frequently asked questions

How many devices does LEVO AG have in the registry?

The registry currently lists 12 devices for LEVO AG. Devices recorded under merged duplicate company entries are counted once.

Which registries list LEVO AG's devices?

Among its 12 most recently registered devices, LEVO AG has devices listed in EUDAMED (8 devices), FDA 510(k) (4 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.

What risk classes do LEVO AG's devices fall under?

Among its 12 most recently registered devices, the classes recorded for LEVO AG's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from LEVO AG in the registry?

The most recently registered devices listed for LEVO AG include C3, LCEV, LEVO MAX and LEVO COMFORT II.

Generated automatically from registry data and not verified by a human reviewer.