FDA applicant
Audio-Aid, Inc.
FDA records 2 decisions for Audio-Aid, Inc. (Mchenry, IL) from 1982 to 1984: 2 510(k) clearances. All are in product code ESD (Hearing Aid, Air-Conduction, Prescription). 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 Audio-Aid, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Audio-Aid, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Audio-Aid, 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) ReportOther applicant names beginning “Audio-Aid”
FDA records each applicant name separately; these may or may not be the same firm.