# Klaxon Mobility GmbH

- Location (FDA's records): Arnoldstein, AT
- FDA decisions: 3 (2022–2025): 3 510(k) clearances
- Names in FDA's records: Klaxon Mobility GmbH (2); Klaxon-Mobility GmbH (1)
- Product codes: ITI (3)
- 510(k) review time since 2016: median 120 days, against 90 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 2 (1 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
- Alber GmbH: 2 (https://510kreport.com/company/alber)

## Firms that cite its devices most
- Batec Mobility, S.L.: 1 (https://510kreport.com/company/batec-mobility)

## Its most-cited devices
- K222502: Klick (Variants: Power, Race, Monster) (2022), cited by 1
- K240267: Klaxon (Twist); Klaxon (Twist R) (2025), cited by 1

## Recent decisions
- K250748: Klaxon (Twist); Klaxon (Twist R) (Apr 11, 2025)
- K240267: Klaxon (Twist); Klaxon (Twist R) (Jan 10, 2025)
- K222502: Klick (Variants: Power, Race, Monster) (Dec 16, 2022)

Source page: https://510kreport.com/company/klaxon-mobility