FDA applicant

Terray Manufacturing, Inc.

Ontario K7s 1l8, CA9 decisions1987–19920 recalls

FDA records 9 decisions for Terray Manufacturing, Inc. (Ontario K7s 1l8, CA) from 1987 to 1992: 9 510(k) clearances. Most are in product codes FSM (Tray, Surgical, Instrument) and HWC (Screw, Fixation, Bone). 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 Terray Manufacturing, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Terray Manufacturing, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Terray 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 “Terray”

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

Terray Corp. 4

Terray Manufacturing, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Terray”