FDA applicant

Symmetry Medical Manufacturing Inc. Dba Tecomet, Inc.

Warsaw, IN1 decision2021–20210 recalls

FDA records 1 decision for Symmetry Medical Manufacturing Inc. Dba Tecomet, Inc. (Warsaw, IN) in 2021: 1 510(k) clearance. All are in product code PHX (Shoulder Prosthesis, Reverse Configuration). 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, orthopedic panel, where it files most

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

FDA decisions per year

1in 2021

2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Symmetry Medical Manufacturing Inc. Dba Tecomet, Inc. by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Symmetry Medical Manufacturing 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 USA, Inc. 1 Symmetry Medical Inc- Manchester 1

Symmetry Medical Manufacturing Inc. Dba Tecomet, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Symmetry”