# Lineus Medical

- Location (FDA's records): Fayetteville, AZ
- FDA decisions: 3 (2022–2023): 3 510(k) clearances
- Names in FDA's records: Lineus Medical (2); Lineus Medical, LLC (1)
- Product codes: QOI (3)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 2 (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
- Site Saver, Inc. D/B/A Lineus Medical: 1 (https://510kreport.com/company/site-saver-d-b-a-lineus-medical)

## Its most-cited devices
- K222791: SafeBreak Vascular (2022), cited by 1
- K223486: SafeBreak® Vascular (2023), cited by 1

## Recent decisions
- K231957: SafeBreak® Vascular (Sep 29, 2023)
- K223486: SafeBreak® Vascular (May 19, 2023)
- K222791: SafeBreak Vascular (Oct 16, 2022)

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