# Telesonic, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 12 (1980–1987): 12 510(k) clearances
- Product codes: ESD (11), IPF (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
- K872606: Telesonic Body Stimulator (Dec 22, 1987)
- K813329: Post-Auricular Hearing Aid Model P-101 (Jan 19, 1982)
- K813330: Post-Auricular Hearing Aid Model S-101 (Jan 19, 1982)
- K813316: Custom-in-the-Ear Hearing Aid (Dec 31, 1981)
- K813344: Post-Auricular Hearing Aid Model Asp-103 (Dec 31, 1981)
- K811031: Telesonic & Arcon (Jul 1, 1981)
- K802597: Telesonic Arcon & Soundex Asp 101 (Nov 12, 1980)
- K802596: Telesonic, Arcon & Soundex Asp 102 (Nov 12, 1980)

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