Coreleader Biotech Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K151204 | HEMO-Bandage | July 31, 2015 |
| K141382 | BIOS KING BIOCELLULOSE FILM | February 10, 2015 |
| K123394 | CORELEADER HYDRO-HEALER HYDROCOLLOID WOUND DRESSING | June 6, 2013 |
| K111578 | CORELEADER COLLA-ALGI FIBER MODEL CAW | September 23, 2011 |
| K111733 | CORELEADER SCAR-DIMMER | September 22, 2011 |
| K102944 | CORELEADER HEMO-PAD MODEL CPII 02030 | September 7, 2011 |
| K102942 | CORELEADER ALGIPLASTER MODEL AP 050501 | June 22, 2011 |
| K102946 | CORELEADER COLLA-PAD MODEL CS 03030 | May 20, 2011 |
| K102943 | CORELEADER ALGI-FIBER WOUND DRESSING MODEL ADW 05050 | April 12, 2011 |