FDA applicant

Orion Industries

Fort Myers, FL1 decision1990–19900 recalls

FDA records 1 decision for Orion Industries (Fort Myers, FL) in 1990: 1 510(k) clearance. All are in product code HFM (Monitor, Uterine Contraction, External (For…). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Orion Industries’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Orion Industries since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Orion”

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

Orion Life Systems, Inc. 33 Orion Diagnostica, Inc. 32 Orion Corp. 21 Orion Diagnostica, Div. Orion Corp. 4 Orion Corporation Soredex 4 Orion Biotech, Inc. 1

Orion Industries

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Orion”