FDA applicant

Symmetry Medical USA, Inc.

Fort Wayne, IN1 decision2004–20040 recalls

FDA records 1 decision for Symmetry Medical USA, Inc. (Fort Wayne, IN) in 2004: 1 510(k) clearance. All are in product code KCT (Sterilization Wrap Containers, Trays…). Its devices cite 3 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Symmetry Medical USA, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Symmetry Medical USA, Inc.’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 “Symmetry”

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

Symmetry Surgical, Inc. 5 Symmetry Medical 3 Symmetry Medical Manufacturing Inc. Dba Tecomet, Inc. 1 Symmetry Medical Inc- Manchester 1

Symmetry Medical USA, Inc.

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 “Symmetry”