# Ind Diagnostics, Inc.

- Location (FDA's records): Delta, B.C., CA
- FDA decisions: 2 (2011–2012): 2 510(k) clearances
- Product codes: KHE (1), LCX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K113506: Ind One Step Occult Blood (Fob) Test (Dec 19, 2012)
- K110889: Ind One Step HCG Urine Pregnancy Test (Strip) (Jun 20, 2011)

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