# Trividia Health, Inc.

- Location (FDA's records): Fort Lauderdale, FL
- FDA decisions: 3 (2016–2026): 3 510(k) clearances
- Names in FDA's records: Trividia Health, Inc. (2); Trividia Health (1)
- Product codes: NBW (2), QRL (1)
- 510(k) review time since 2016: median 189 days, against 190 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Roche Diabetes Care, Inc.: 1 (https://510kreport.com/company/roche-diabetes-care)
- Nipro Diagnostics, Inc.: 1 (https://510kreport.com/company/nipro-diagnostics)

## Recent decisions
- K262116: TRUE METRIX Self Monitoring Blood Glucose System (Jul 23, 2026)
- K221072: TRUEdraw Lancing Device, Mini Lancing Device (Oct 18, 2022)
- K143548: TRUE METRIX GO Self Monitoring Blood Glucose System (Apr 1, 2016)

Source page: https://510kreport.com/company/trividia-health