# New Eder Corp.

- Location (FDA's records): Elk Groove Village, IL
- FDA decisions: 4 (1994–1995): 4 510(k) clearances
- Product codes: HET (2), GEI (1), KNF (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
- K941206: Dual Valve Aspiration/Lavage Cannula and Aspiration/Suction Probe (Jul 25, 1995)
- K941435: Bipolar U-Shape Handle, Prongs, and Cord (Apr 11, 1995)
- K941207: Monopolar Suction Cannula; Monopolar Electrodes (Jan 24, 1995)
- K941208: Diagnostic Sleeve, Reducer Sleeve (Jun 17, 1994)

Source page: https://510kreport.com/company/new-eder