510(k) Report

FDA applicant

Belport Co., Inc.

Mchenry, IL2 decisions1981–19820 recalls

FDA records 2 decisions for Belport Co., Inc. (Mchenry, IL) from 1981 to 1982: 2 510(k) clearances. Most are in product codes ELW (Material, Impression) and JES (Floss, Dental). 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 Belport Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Belport Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • ELWMaterial, Impression1decision
  • JESFloss, Dental1decision

What has FDA decided for it lately?

  • K820061Reversible Hydrocolloid Impression MatBelport Co., Inc. · 1982
  • K812120Gingi-Plain Cords & BraidsBelport Co., Inc. · 1981

All 2 as Belport Co., Inc. →

Other applicant names beginning “Belport”

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

Belport Company, Inc., Gingi-Pak 11The Belport Company Inc., DBA Gingi-Pak 1