Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in South KoreaLabelled 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 14, 2026, FDA's public records list Genoss with 23 510(k) clearances. The most recent is a 510(k) clearance dated May 5, 2025: Bluemoon.
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.
| May 5, 2025 | BluemoonK242386 · EBZ | 510(k) clearances |
| Aug 9, 2024 | The TrustK222688 · EKX | 510(k) clearances |
| Jun 21, 2024 | rainbow Paste Stain SEK233885 · EIH | 510(k) clearances |
| Feb 23, 2024 | rainbowTM Multi-Layer Block / bright 3-Layer / bright MonoK232174 · EIH | 510(k) clearances |
| Jul 28, 2023 | Bright MTA Sealer PlusK231480 · KIF | 510(k) clearances |
| Dec 15, 2022 | Bright Impress-Light, Bright Impress-Medium, Bright Impress-Heavy, Bright Impress-Bite, Bright Impress-PuttyK214086 · ELW | 510(k) clearances |
| Nov 30, 2020 | Bright High FlowK200155 · EBF | 510(k) clearances |
| Oct 28, 2020 | Bright Bond UniversalK200153 · KLE | 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
