# Grindguard, Inc.

- Location (FDA's records): San Francisco, CA
- FDA decisions: 2 (2025–2026): 2 510(k) clearances
- Product codes: MQC (1), SHI (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (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
- Lijia, LLC: 1 (https://510kreport.com/company/lijia)
- Prevest Denpro Limited: 1 (https://510kreport.com/company/prevest-denpro)

## Firms that cite its devices most
- ClearClub: 1 (https://510kreport.com/company/clearclub)

## Its most-cited devices
- K251724: Remi Impression Material (2026), cited by 1

## Recent decisions
- K251724: Remi Impression Material (Feb 25, 2026)
- K243516: Remi Custom Night Guard (Feb 10, 2025)

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