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 Coreleader Biotech Co., Ltd. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jul 31, 2015: HEMO-Bandage.
| Jul 31, 2015 | HEMO-BandageK151204 · QSY | 510(k) clearances |
| Feb 10, 2015 | BIOS KING BIOCELLULOSE FILMK141382 · FRO | 510(k) clearances |
| Jun 6, 2013 | CORELEADER HYDRO-HEALER HYDROCOLLOID WOUND DRESSINGK123394 · FRO | 510(k) clearances |
| Sep 23, 2011 | CORELEADER COLLA-ALGI FIBER MODEL CAWK111578 · FRO | 510(k) clearances |
| Sep 22, 2011 | CORELEADER SCAR-DIMMERK111733 · MDA | 510(k) clearances |
| Sep 7, 2011 | CORELEADER HEMO-PAD MODEL CPII 02030K102944 · QSY | 510(k) clearances |
| Jun 22, 2011 | CORELEADER ALGIPLASTER MODEL AP 050501K102942 · FRO | 510(k) clearances |
| May 20, 2011 | CORELEADER COLLA-PAD MODEL CS 03030K102946 · KGN | 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
