FDA applicant
Erich Jaeger, Inc.
FDA records 40 decisions for Erich Jaeger, Inc. (Mchenry, IL) from 1984 to 2003: 40 510(k) clearances. Most are in product codes BZC (Calculator, Pulmonary Function Data) and BZG (Spirometer, Diagnostic). Its devices cite 2 predicates, 2 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Erich Jaeger GmbH”, “Erich Jaeger GmbH & Co. KG”, “Erich Jaeger B.V.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Erich Jaeger, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Erich Jaeger, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Erich Jaeger, Inc.’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