FDA applicant
New Eder Corp.
FDA records 4 decisions for New Eder Corp. (Elk Groove Village, IL) from 1994 to 1995: 4 510(k) clearances. Most are in product codes HET (Laparoscope, Gynecologic (And Accessories)) and GEI (Electrosurgical, Cutting & Coagulation &…). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided New Eder Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for New Eder Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like New Eder Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report