FDA applicant

Mrlb Intl., Inc.

Fergus Falls, MN3 decisions1997–19990 recalls

FDA records 3 decisions for Mrlb Intl., Inc. (Fergus Falls, MN) from 1997 to 1999: 3 510(k) clearances. All are in product code EIA (Unit, Operative Dental). Its devices cite 3 predicates, 2 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, dental panel, where it files most

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

FDA decisions per year

No FDA decision for Mrlb Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mrlb Intl., Inc.’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

Mrlb Intl., Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?