FDA applicant

Medvice Consulting, Inc.

Grand Junction, CO1 decision2000–20000 recalls

FDA records 1 decision for Medvice Consulting, Inc. (Grand Junction, CO) in 2000: 1 510(k) clearance. All are in product code LPL (Lenses, Soft Contact, Daily Wear). 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, ophthalmic panel, where it files most

How often FDA has decided Medvice Consulting, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medvice Consulting, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medvice Consulting, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?