# American Ortomed Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 6 (1978–1985): 6 510(k) clearances
- Product codes: KWA (2), JDG (1), JDK (1), KWL (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
- K842466: Titanium Mittelmeier Type Acetabular (Jan 30, 1985)
- K842518: Uniloc-Cementless & Self Tap Acetabular (Jan 30, 1985)
- K842465: Uniloc (Nov 19, 1984)
- K840413: Cement Restrictor (Mar 5, 1984)
- K820719: The Icr Knee (May 12, 1982)
- K780497: Spheristem Total Hip Prosthesis (Jun 14, 1978)

Source page: https://510kreport.com/company/american-ortomed