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 14, 2026, FDA's public records list Filmecc with 6 510(k) clearances. The most recent is a 510(k) clearance dated Sep 3, 2026: CROSSLEAD Standard 035 and CROSSLEAD Stiff 035.
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.
| Sep 3, 2026 | CROSSLEAD Standard 035 and CROSSLEAD Stiff 035K261281 · DQX | 510(k) clearances |
| Mar 9, 2023 | Vassallo GT 018 HybridK223432 · DQX | 510(k) clearances |
| Oct 26, 2022 | VASSALLO GT EXTK222631 · DQX | 510(k) clearances |
| Jun 30, 2022 | VASSALLO GT 018 FloppyK213949 · DQX | 510(k) clearances |
| May 4, 2021 | VASSALLO GT HybridK203529 · DQX | 510(k) clearances |
| Apr 21, 2021 | VASSALLO GTK203533 · DQX | 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
