FDA applicant

Pantheon Products, Inc.

Odessa, TX1 decision1986–19860 recalls

FDA records 1 decision for Pantheon Products, Inc. (Odessa, TX) in 1986: 1 510(k) clearance. All are in product code HMP (Pad, Eye). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Pantheon Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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See the 510(k) Report

Other applicant names beginning “Pantheon”

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

Pantheon Spinal 4 Pantheon Medical 1 Pantheon Surgical Products 1 Pantheon Research 1

Pantheon Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Pantheon”