# Bosch Healthcare Solutions GmbH

- Location (FDA's records): Waiblingen, DE
- FDA decisions: 2 (2024–2025): 2 510(k) clearances
- Product codes: MXA (2)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K233775: Vivatmo pro (2024), cited by 1

## Recent decisions
- K243926: Vivatmo pro-S (Sep 11, 2025)
- K233775: Vivatmo pro (Feb 22, 2024)

Source page: https://510kreport.com/company/bosch-healthcare-solutions