FDA applicant

Medoc Ltd. Advanced Medical Systems

Somerset, MA4 decisions2001–20060 recalls

FDA records 4 decisions for Medoc Ltd. Advanced Medical Systems (Somerset, MA) from 2001 to 2006: 4 510(k) clearances. Most are in product codes NTU (Evoked Potential Stimulator, Thermal) and LLN (Device, Vibration Threshold Measurement). Its devices cite 4 predicates, 3 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, neurology panel, where it files most

How often FDA has decided Medoc Ltd. Advanced Medical Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medoc Ltd. Advanced Medical Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medoc Ltd. Advanced Medical Systems’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 “Medoc”

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

Medoc Corp. 1

Medoc Ltd. Advanced Medical Systems

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 “Medoc”