FDA applicant

Nexan Telemed, Ltd.

Rockville, MD1 decision1999–19990 recalls

FDA records 1 decision for Nexan Telemed, Ltd. (Rockville, MD) in 1999: 1 510(k) clearance. All are in product code MWJ (Electrocardiograph, Ambulatory (Without…). Its devices cite 6 predicates, 0 of them its own earlier devices. 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, cardiovascular panel, where it files most

How often FDA has decided Nexan Telemed, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nexan Telemed, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Nexan”

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

Nexan, Ltd. 2

Nexan Telemed, Ltd.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Nexan”