FDA applicant

Oms Medico, Inc.

Braintree, MA7 decisions1987–19870 recalls

FDA records 7 decisions for Oms Medico, Inc. (Braintree, MA) in 1987: 7 510(k) clearances. All are in product code GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Oms Medico, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Oms Medico, Inc.

Which product codes does it file in?

What has FDA decided for it lately?