# Smartguard Rx, Inc.

- Location (FDA's records): Layton, UT
- FDA decisions: 1 (2021–2021): 1 510(k) clearance
- Product codes: LRK (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
- Apnea Sciences Corporation: 1 (https://510kreport.com/company/apnea-sciences)

## Firms that cite its devices most
- Oscimed SA: 1 (https://510kreport.com/company/oscimed)
- Oniris: 1 (https://510kreport.com/company/oniris)

## Its most-cited devices
- K200657: SmartGuard Anti-Snoring Device (2021), cited by 2

## Recent decisions
- K200657: SmartGuard Anti-Snoring Device (Aug 23, 2021)

Source page: https://510kreport.com/company/smartguard-rx