FDA applicant

Terray Corp.

Arnprior, CA4 decisions1998–20070 recalls

FDA records 4 decisions for Terray Corp. (Arnprior, CA) from 1998 to 2007: 4 510(k) clearances. Most are in product codes HRS (Plate, Fixation, Bone) and KWD (Prosthesis, Toe, Hemi-, Phalangeal). 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 Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Terray”

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

Terray Manufacturing, Inc. 9

Terray Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Terray”