FDA applicant

Almore Intl., Inc.

Portland, OR21 decisions1980–19860 recalls

FDA records 21 decisions for Almore Intl., Inc. (Portland, OR) from 1980 to 1986: 21 510(k) clearances. Most are in product codes EJL (Bur, Dental) and HTD (Forceps). 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 Almore Intl., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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Almore Intl., Inc.

Which product codes does it file in?

What has FDA decided for it lately?