510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K111733Substantially Equivalent

Coreleader Scar-Dimmer

Coreleader Biotech Co., Ltd, New Taipei, Taiwan, TW / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K111733 is the FDA 510(k) clearance record for CORELEADER SCAR-DIMMER, a class I device, cleared for Coreleader Biotech Co., Ltd. on under FDA product code MDA (Elastomer, Silicone, For Scar Management). FDA records list 9 510(k) clearances for Coreleader Biotech Co., Ltd., from to . As of , FDA records show no recalls naming K111733.

Clearance record

Decision date
Received
(93 days to decision)
Product code
MDA Elastomer, Silicone, For Scar Management
Regulation
21 CFR 878.4025
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Coreleader Biotech Co., Ltd. 19f # 100, Sec 1, New Taipei, Taiwan, TW
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MDA

Trailing 12 months

FDA records hold no clearances under product code MDA in the trailing twelve months.

FDA records show no clearances under product code MDA in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MDA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260