FDA applicant

Kerr Hearing Aid Laboratory

Titusville, FL1 decision1987–19870 recalls

FDA records 1 decision for Kerr Hearing Aid Laboratory (Titusville, FL) in 1987: 1 510(k) clearance. 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, last Nov 3, 2026

FIG. A — Illustration, ear, nose and throat panel, where it files most

How often FDA has decided Kerr Hearing Aid Laboratory’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kerr Hearing Aid Laboratory since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Kerr Hearing Aid Laboratory by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Kerr Hearing Aid Laboratory’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

Other applicant names beginning “Kerr”

FDA records each applicant name separately; these may or may not be the same firm.

Kerr Corporation 41 Kerr Corporation (Danbury) 32 Kerr Dental Materials Center 17

Kerr Hearing Aid Laboratory

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Kerr”