FDA applicant

Promed Corp.

Mchenry, IL4 decisions1978–19920 recalls

FDA records 4 decisions for Promed Corp. (Mchenry, IL) from 1978 to 1992: 4 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and KOI (Stimulator, Nerve, Peripheral, Electric). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Promed Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Promed”

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

Promed Advance Technology Co., Ltd. 1

Promed Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Promed”