FDA applicant

Diagnostic Group, Dba Grason-Stadler

Eden Prairie, MN1 decision2015–20150 recalls

FDA records 1 decision for Diagnostic Group, Dba Grason-Stadler (Eden Prairie, MN) in 2015: 1 510(k) clearance. All are in product code ETY (Tester, Auditory Impedance). 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 Diagnostic Group, Dba Grason-Stadler’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2015high 1 (2015) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — Diagnostic Group, Dba Grason-Stadler by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Diagnostic”

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

Diagnostic Products Corp. 324 Diagnostic Systems Laboratories, Inc. 94 Diagnostic Chemicals, Ltd. (Usa) 77 Diagnostic Reagents, Inc. 66 Diagnostic Chemicals, Ltd. 66 Diagnostic Hybrids, Inc. 37 Diagnostic Technology, Inc. 28 Diagnostic Solutions, Inc. 26 Diagnostic Ultrasound Corp. 16 Diagnostic Systems 14 Diagnostic Reagent Tech. 10 Diagnostic Specialties 8

Diagnostic Group, Dba Grason-Stadler

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Diagnostic”