510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K920357Substantially Equivalent

Ultracell Ear Wick

Ultracell Medical Technologies, Inc., North Stonington CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K920357 is the FDA 510(k) clearance record for ULTRACELL EAR WICK, a class I device, cleared for Ultracell Medical Technologies, Inc. on under FDA product code KCN (Ear Wick). FDA records list 24 510(k) clearances for Ultracell Medical Technologies, Inc., from to . As of , FDA records show 6 recalls naming K920357.

Clearance record

Decision date
Received
(371 days to decision)
Product code
KCN Ear Wick
Regulation
21 CFR 874.5220
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Ultracell Medical Technologies, Inc. P.O. Box 326, North Stonington CT
510(k) summary
Statement
Third party review
No

Clearances, product code KCN

Trailing 12 months

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

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