# Xstrahl, Ltd.

- Location (FDA's records): Brownhills, GB
- FDA decisions: 3 (2017–2024): 3 510(k) clearances
- Product codes: JAD (2), MUJ (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Sensus Healthcare, Inc.: 1 (https://510kreport.com/company/sensus-healthcare)
- Lifeline Software, Inc.: 1 (https://510kreport.com/company/lifeline-software)

## Its most-cited devices
- K172080: Photoelectric Therapy System (2017), cited by 1

## Recent decisions
- K240671: XBeam (v2) (Dec 4, 2024)
- K230611: X80 / RADiant / PhotoElectric Therapy System  (RADiant Aura) (Jul 13, 2023)
- K172080: Photoelectric Therapy System (Sep 29, 2017)

Source page: https://510kreport.com/company/xstrahl