Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Belport Company with 4 510(k) clearances. The most recent is a 510(k) clearance dated Oct 27, 2026: AquaVance Clear Fluoride Treatment.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Oct 27, 2026 | AquaVance Clear Fluoride TreatmentK262775 · LBH | 510(k) clearances |
| Aug 7, 2026 | PacTemp Automix NEK261937 · EMA | 510(k) clearances |
| Feb 22, 1982 | REVERSIBLE HYDROCOLLOID IMPRESSION MATK820061 · ELW | 510(k) clearances |
| Sep 8, 1981 | GINGI-PLAIN CORDS & BRAIDSK812120 · JES | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
