FDA applicant

Symmetry Medical

New Bedford, MA3 decisions2002–20123 recalls

FDA records 3 decisions for Symmetry Medical (New Bedford, MA) from 2002 to 2012: 3 510(k) clearances. Most are in product codes FRG (Wrap, Sterilization) and KCT (Sterilization Wrap Containers, Trays…). Its devices cite 5 predicates, 0 of them its own earlier devices. 3 recalls are linked to its devices.

FDA’s records also spell it “Symmetry Medical, Inc.”.

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’s devices, and how often a recall has named them.

FDA decisions per year

2in 2012

2007high 2 (2012) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

3in 2016

2007high 3 (2016) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Symmetry Medical’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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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 USA, Inc. 1 Symmetry Medical Manufacturing Inc. Dba Tecomet, Inc. 1 Symmetry Medical Inc- Manchester 1

Symmetry Medical

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?

What has been recalled?

Other applicant names beginning “Symmetry”