FDA applicant

Austin Miller Trauma, LLC

Germantown, TN1 decision2019–20190 recalls

FDA records 1 decision for Austin Miller Trauma, LLC (Germantown, TN) in 2019: 1 510(k) clearance. All are in product code KTT (Appliance, Fixation, Nail/Blade/Plate…). Its devices cite 4 predicates, 0 of them its own earlier devices. 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, orthopedic panel, where it files most

How often FDA has decided Austin Miller Trauma, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2019

2019high 1 (2019) · low 0 (2020)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2019.

FIG. 1 — Austin Miller Trauma, LLC by year, 2019–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Austin”

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

Austin Biological Laboratories 45 Austin Assoc. 1 Austin Medical, Inc. 1 Austin & Associates, Inc./Telos Medical Equipment 1 Austin Medical Ventures, Inc. 1 The Austin-Lenick Co. 1

Austin Miller Trauma, LLC

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Austin”