# Orthion Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 11 (1981–1983): 11 510(k) clearances
- Product codes: IKX (2), ILS (2), INQ (1), INW (1), ITJ (1), INM (1), ILE (1), IPF (1), IYM (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
- K832546: Mark V High Voltage Galvanic Stimulatorr (Oct 14, 1983)
- K823150: Sesam Treatment Table (Nov 5, 1982)
- K823149: OB Tilt Table (Nov 5, 1982)
- K823105: Resi-Walker (Nov 5, 1982)
- K823153: Bath Tub Seat & Bath Board (Nov 5, 1982)
- K823151: OB Tripp Transport Chair (Nov 5, 1982)
- K823156: Collapsable Lavatory Heightener (Nov 5, 1982)
- K823155: Lavatory Seat Heightener (Nov 5, 1982)

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