# Staodynamics, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 14 (1979–1985): 14 510(k) clearances
- Product codes: GZJ (4), IPF (3), GXY (3), BWJ (2), IMA (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
- K852298: Tens-Aid Sterile Electrodes for Post-OP Tens (Jun 24, 1985)
- K843964: Tens-Aid Premium Electrodes (Feb 25, 1985)
- K832988: Staodyn Ems/Plus (Nov 22, 1983)
- K813283: 10D (Tens Device) (Feb 10, 1982)
- K813098: Tens Device (Nov 20, 1981)
- K811345: Insight (Jul 10, 1981)
- K792529: Point Locator Stimulator (Feb 26, 1980)
- K792501: PLS Mini (Feb 26, 1980)

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