510(k) Report

FDA applicant

Oriental Medical Supplies, Inc.

Braintree, MA6 decisions1985–19890 recalls

FDA records 6 decisions for Oriental Medical Supplies, Inc. (Braintree, MA) from 1985 to 1989: 6 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and IMD (Pack, Hot Or Cold, Disposable). 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 Oriental Medical Supplies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Oriental Medical Supplies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Oriental Medical Supplies, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Oriental”

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