# Alexotek Co.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 4 (1984–1988): 4 510(k) clearances
- Product codes: DZD (2), EJF (2)
- 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
- K881789: Miniline Bracket (Jun 1, 1988)
- K834446: Alexotek Lingual Tubes (Apr 5, 1984)
- K834392: Labial Cuspid Tube (Feb 28, 1984)
- K834272: Alexolok Bracket (Feb 3, 1984)

Source page: https://510kreport.com/company/alexotek