# True Diagnostics, Inc.

- Location (FDA's records): Carlsbad, CA
- FDA decisions: 2 (2017–2019): 2 510(k) clearances
- Product codes: JHI (1), LCX (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
- Church & Dwight Co., Inc.: 2 (https://510kreport.com/company/church-dwight)

## Recent decisions
- K182328: VeriClear Digital Early Result Pregnancy Test (May 15, 2019)
- K172257: TrueDX hCG Early Result Pregnancy Test (Midstream Format), TrueDX hCG Early Result Pregnancy Test (Cassette Format), VeriClear Early Result Pregnancy Test (Midstream Format), VeriClear Early Result Pregnancy Test (Cassette Format) (Dec 22, 2017)

Source page: https://510kreport.com/company/true-diagnostics