Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ChinaLabelled 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 Sichuan Prius Biotechnology with 9 510(k) clearances. The most recent is a 510(k) clearance dated Nov 21, 2022: Infusion Sets 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.
| Nov 21, 2022 | Infusion Sets for Single UseK221075 · FPA | 510(k) clearances |
| Nov 21, 2022 | Intravenous Needles for Single Use,Safety Intravenous Needles for Single UseK221078 · FPA | 510(k) clearances |
| Nov 21, 2022 | Infusion Sets for Single Use with NeedlesK221069 · FPA | 510(k) clearances |
| Oct 4, 2022 | Sterile Hypodermic Syringes for Single UseK221079 · FMF | 510(k) clearances |
| Oct 4, 2022 | Sterile Hypodermic Needles for Single UseK221066 · FMI | 510(k) clearances |
| Oct 4, 2022 | Sterile Safety Hypodermic Needles for Single UseK221080 · FMI | 510(k) clearances |
| Oct 4, 2022 | Sterile Hypodermic Syringes for Single Use with NeedlesK221068 · FMF | 510(k) clearances |
| Oct 4, 2022 | Sterile Hypodermic Syringes for Single Use with Safety NeedlesK221073 · MEG | 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
