# Xtrallux, LLC

- Location (FDA's records): Miami, FL
- FDA decisions: 1 (2022–2022): 1 510(k) clearance
- Product codes: OAP (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (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
- Capillus, LLC: 2 (https://510kreport.com/company/capillus)

## Recent decisions
- K222364: Xtrallux Alpha (XA136R-USA), Xtrallux Super Plus (XS276R-USA/XS276L-USA), Xtrallux Turbo Pro (XP316R-USA), Xtrallux Extreme RX (XR352R-USA) (Nov 16, 2022)

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