FDA applicant

The Surgeon General, Department of the Army (TSG-DA)

Fort Dietrick, MD2 decisions2024–20260 recalls

FDA records 2 decisions for The Surgeon General, Department of the Army (TSG-DA) (Fort Dietrick, MD) from 2024 to 2026: 2 510(k) clearances. Most are in product codes SAR (Adjunctive Hemodynamic Indicator With Decision…) and GXN (Plate, Cranioplasty, Preformed, Non-Alterable). Its devices cite 2 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, cardiovascular panel, where it files most

How often FDA has decided The Surgeon General, Department of the Army (TSG-DA)’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2024high 1 (2024) · low 0 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2024.

FIG. 1 — The Surgeon General, Department of the Army (TSG-DA) by year, 2024–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like The Surgeon General, Department of the…’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 “The”

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

Surgeon Surgical Instrumentation, Inc. 10 The Surgeon General, Department of the Army 2 Surgeon Design 1

The Surgeon General, Department of the Army (TSG-DA)

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “The”