# Diatron U.S., Inc.

- Location (FDA's records): Lenexa, KS
- FDA decisions: 3 (2012–2016): 3 510(k) clearances
- Product codes: GKZ (2), CFR (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Abbott Laboratories: 2 (https://510kreport.com/company/abbott-laboratories)
- Diatron Group: 1 (https://510kreport.com/company/diatron-group)

## Recent decisions
- K151487: Diatron Pictus 700 Clinical Chemistry Analyzer, Diatron ISE,  Diatron Glucose Hexokinase Method (Jan 14, 2016)
- K111534: Abacus 3CP (Aug 2, 2012)
- K112755: Abacus 5 (Mar 27, 2012)

Source page: https://510kreport.com/company/diatron-us