Coreleader Biotech Co., Ltd. is one of 180 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Coreleader Biotech Co., Ltd. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Coreleader Biotech Co., Ltd. has 9 FDA 510(k) cleared medical devices. Based in Taipei, Taiwan, TW.
Historical record: 9 cleared submissions from 2011 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Coreleader Biotech Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Coreleader Biotech Co., Ltd.
9 devices
Cleared
Jul 31, 2015
HEMO-Bandage
General & Plastic Surgery
87d
Cleared
Feb 10, 2015
BIOS KING BIOCELLULOSE FILM
General & Plastic Surgery
259d
Cleared
Jun 06, 2013
CORELEADER HYDRO-HEALER HYDROCOLLOID WOUND DRESSING
General & Plastic Surgery
216d
Cleared
Sep 23, 2011
CORELEADER COLLA-ALGI FIBER MODEL CAW
General & Plastic Surgery
108d
Cleared
Sep 22, 2011
CORELEADER SCAR-DIMMER
General & Plastic Surgery
93d
Cleared
Sep 07, 2011
CORELEADER HEMO-PAD MODEL CPII 02030
General & Plastic Surgery
338d
Cleared
Jun 22, 2011
CORELEADER ALGIPLASTER MODEL AP 050501
General & Plastic Surgery
261d
Cleared
May 20, 2011
CORELEADER COLLA-PAD MODEL CS 03030
General & Plastic Surgery
228d
Cleared
Apr 12, 2011
CORELEADER ALGI-FIBER WOUND DRESSING MODEL ADW 05050
General & Plastic Surgery
190d