510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K781147Substantially Equivalent

Epilator, Ease-Multi-Mode

Greenleaf-Carter Enterprises, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K781147 is the FDA 510(k) clearance record for EPILATOR, EASE-MULTI-MODE, a class I device, cleared for Greenleaf-Carter Enterprises, Inc. on under FDA product code KCW (Epilator, High Frequency, Needle-Type). FDA records list one 510(k) clearance for Greenleaf-Carter Enterprises, Inc. As of , FDA records show no recalls naming K781147.

Clearance record

Decision date
Received
(92 days to decision)
Product code
KCW Epilator, High Frequency, Needle-Type
Regulation
21 CFR 878.5350
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Greenleaf-Carter Enterprises, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KCW

Trailing 12 months

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

FDA records show no clearances under product code KCW in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KCW, 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