FDA applicant

Engineered Medical Technology, Inc.

Victoria, TX1 decision2001–20010 recalls

FDA records 1 decision for Engineered Medical Technology, Inc. (Victoria, TX) in 2001: 1 510(k) clearance. All are in product code CBF (Chamber, Hyperbaric). 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, anesthesiology panel, where it files most

How often FDA has decided Engineered Medical Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Engineered Medical Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Engineered Medical Technology, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Engineered”

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

Engineered Medical Systems 24 Engineered Medical Solutions Co., LLC 2 Engineered Orthopedic Technologies, Inc. 2 Engineered Tissue Solutions, LLC 1 Engineered Endodontics 1 Engineered Custom Mfg., Inc. 1

Engineered Medical Technology, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Engineered”