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 Wepon Medical Technology with 5 510(k) clearances. The most recent is a 510(k) clearance dated Sep 8, 2023: Sterile Safety Hypodermic Needles for Single Use.
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 8, 2023 | Sterile Safety Hypodermic Needles for Single UseK231723 · FMI | 510(k) clearances |
| Sep 8, 2023 | Sterile Auto-Disable Syringes with/without Needle for Single UseK231727 · FMF | 510(k) clearances |
| Sep 8, 2023 | Sterile Hypodermic Needles for Single UseK231720 · FMI | 510(k) clearances |
| Sep 8, 2023 | Sterile syringes for single use with/without needleK231729 · FMI | 510(k) clearances |
| Jan 4, 2022 | Medical Surgical MaskK212299 · FXX | 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
