FDA applicant

The Telos Co.

Walker, MI2 decisions1981–19810 recalls

FDA records 2 decisions for The Telos Co. (Walker, MI) in 1981: 2 510(k) clearances. Most are in product codes KQW (Goniometer, Nonpowered) and HST (Apparatus, Traction, Non-Powered). 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 The Telos Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Telos Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like The Telos Co.’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 “The”

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

Telos Medical Corp. 7 Telos Medical Equipment 1

The Telos Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “The”