# Magnus Medical, Inc.

- Location (FDA's records): Burlingame, CA
- FDA decisions: 1 (2022–2022): 1 510(k) clearance
- Product codes: OBP (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (0 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
- Nexstim OY: 1 (https://510kreport.com/company/nexstim)

## Firms that cite its devices most
- Brainsway, Ltd.: 1 (https://510kreport.com/company/brainsway)
- Tonica Elektronik A/S: 1 (https://510kreport.com/company/tonica-elektronik-a-s)

## Its most-cited devices
- K220177: Magnus Neuromodulation System (MNS) with SAINT Technology, Model Number 1001K (2022), cited by 2

## Recent decisions
- K220177: Magnus Neuromodulation System (MNS) with SAINT Technology, Model Number 1001K (Sep 1, 2022)

Source page: https://510kreport.com/company/magnus-medical