# Endomedics, Inc.

- Location (FDA's records): Walker, MI
- FDA decisions: 4 (1984–1984): 4 510(k) clearances
- Product codes: JDL (1), KWL (1), JDI (1), KXA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Biocore9, LLC: 1 (https://510kreport.com/company/biocore9)

## Its most-cited devices
- K842202: New Jersey Acetabular Component & (1984), cited by 1

## Recent decisions
- K831792: Self-Aligning Acetabular Component (Sep 20, 1984)
- K842234: New Jersey Femoral Stem (Jul 20, 1984)
- K842202: New Jersey Acetabular Component & (Jul 20, 1984)
- K842233: New Jersey Femoral Resurfacing Component (Jul 20, 1984)

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