FDA applicant

Engineered Orthopedic Technologies, Inc.

San Clemente, CA2 decisions1988–19940 recalls

FDA records 2 decisions for Engineered Orthopedic Technologies, Inc. (San Clemente, CA) from 1988 to 1994: 2 510(k) clearances. Most are in product codes HBL (Holder, Head, Neurosurgical (Skull Clamp)) and KDP (Regulator, Vacuum). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Engineered Orthopedic Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Engineered Orthopedic Technologies, 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 Medical Technology, Inc. 1 Engineered Tissue Solutions, LLC 1 Engineered Endodontics 1 Engineered Custom Mfg., Inc. 1

Engineered Orthopedic Technologies, 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”