FDA applicant

Zygo Industries, Inc.

Portland, OR6 decisions1987–19930 recalls

FDA records 6 decisions for Zygo Industries, Inc. (Portland, OR) from 1987 to 1993: 6 510(k) clearances. Most are in product codes ILQ (System, Communication, Powered) and LEL (Device, Sleep Assessment). 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 Zygo Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Zygo Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Zygo”

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

Zygo Corp. 1

Zygo Industries, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Zygo”