FDA applicant

Companion Products Intl.

Coyote, CA2 decisions1991–19910 recalls

FDA records 2 decisions for Companion Products Intl. (Coyote, CA) in 1991: 2 510(k) clearances. All are in product code ILQ (System, Communication, 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, physical medicine panel, where it files most

How often FDA has decided Companion Products Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Companion Products Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Companion”

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

Companion Medical, Inc. 5 Companion Spine France 4

Companion Products Intl.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Companion”