FDA applicant

Laborie Medical Tech Corp.

Williston, VT6 decisions1994–19990 recalls

FDA records 6 decisions for Laborie Medical Tech Corp. (Williston, VT) from 1994 to 1999: 6 510(k) clearances. Most are in product codes KPI (Stimulator, Electrical, Non-Implantable, For…) and LIL (Monitor, Penile Tumescence). No recall is linked to its devices.

FDA’s records also spell it “Laborie Medical Tech, Inc.”.

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 Laborie Medical Tech Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Laborie Medical Tech Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Laborie Medical Tech Corp.’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 “Laborie”

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

Laborie Medical Technologies, Ltd. 18

Laborie Medical Tech Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Laborie”