# Adi Diagnostics, Inc.

- Location (FDA's records): Rexdale, Ontario, CA
- FDA decisions: 4 (1989–1991): 4 510(k) clearances
- Product codes: GTZ (1), LJC (1), LIP (1), GMQ (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: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K910487: Visuwell Syphilis Antigen (Jun 24, 1991)
- K900973: Visuwell (R) Chlamydia (May 15, 1990)
- K900338: Visuwell (R) Reagin Test (Modification) (Apr 10, 1990)
- K890840: Visuwell Group a Streptococcus Detection Kit (Mar 27, 1989)

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