510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K772390Substantially Equivalent

Day Ear Hook

Edward Weck, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K772390 is the FDA 510(k) clearance record for DAY EAR HOOK, a class I device, cleared for Edward Weck, Inc. on under FDA product code JYL (Hook, Microsurgical Ear). FDA records list 140 510(k) clearances for Edward Weck, Inc., from to . As of , FDA records show no recalls naming K772390.

Clearance record

Decision date
Received
(21 days to decision)
Product code
JYL Hook, Microsurgical Ear
Regulation
21 CFR 874.4420
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Edward Weck, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code JYL

Trailing 12 months

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

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