Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Belport Company, Inc., Gingi-Pak with 11 510(k) clearances. The most recent is a 510(k) clearance dated Apr 10, 2026: Porcelain Etch Gel.
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.
| Apr 10, 2026 | Porcelain Etch GelK260430 · KLE | 510(k) clearances |
| Sep 2, 2025 | RODIN CementK251775 · EMA | 510(k) clearances |
| Jul 2, 2025 | RC-SwiftPrepK250279 · KJJ | 510(k) clearances |
| May 7, 2025 | SDF ProK250222 · PHR | 510(k) clearances |
| Jun 20, 2024 | RODIN Titan 3D ResinK240688 · EBI | 510(k) clearances |
| Jun 13, 2024 | ProMin Dental Desensitizing GelK231060 · LBH | 510(k) clearances |
| Mar 26, 2024 | RODIN 3D Resin SPLINT, Hard/FlexK231793 · MQC | 510(k) clearances |
| Mar 27, 2023 | RODIN Palette Naturalizing KitK223365 · EBD | 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
