# Activatek, Inc.

- Location (FDA's records): West Valley, UT
- FDA decisions: 3 (2006–2014): 3 510(k) clearances
- Product codes: EGJ (3)
- Predicates its devices cite: 7 (2 its own); citations of its devices by later devices: 2 (2 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
- Empi: 2 (https://510kreport.com/company/empi)
- Iomed, Inc.: 2 (https://510kreport.com/company/iomed)
- Naimco, Inc.: 1 (https://510kreport.com/company/naimco)

## Its most-cited devices
- K061522: Trivarion Buffered Iontophoresis Electrode System (2006), cited by 2

## Recent decisions
- K132832: Activapatch ET Iontophoresis Patch (Feb 13, 2014)
- K091326: Activapatch (May 27, 2009)
- K061522: Trivarion Buffered Iontophoresis Electrode System (Aug 1, 2006)

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