510(k) Report

FDA applicant

Medical Innovative Products

Hopkonton, MA1 decision2003–20030 recalls

FDA records 1 decision for Medical Innovative Products (Hopkonton, MA) in 2003: 1 510(k) clearance. All are in product code KNT (Tubes, Gastrointestinal (And Accessories)). Its devices cite 3 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, gastroenterology and urology panel, where it files most

How often FDA has decided Medical Innovative Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Innovative Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medical Innovative Products’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • KNTTubes, Gastrointestinal (And Accessories)1decision

Whose devices does it build on?

Its devices cite 3 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K022558NGTMedical Innovative Products · 2003

The one decision as Medical Innovative Products →