FDA applicant

Contec Medical Vision, Ltd.

Fallston,, MD2 decisions1998–19980 recalls

FDA records 2 decisions for Contec Medical Vision, Ltd. (Fallston,, MD) in 1998: 2 510(k) clearances. All are in product code GCT (Light Source, Endoscope, Xenon Arc). Its devices cite 7 predicates, 1 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, gastroenterology and urology panel, where it files most

How often FDA has decided Contec Medical Vision, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Contec Medical Vision, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Contec Medical Vision, 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 “Contec”

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

Contec Medical System Co., Ltd. 12 Contec Medical Systems Co.,Ltd 12

Contec Medical Vision, Ltd.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Contec”