510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K071178Substantially Equivalent

Otomedics Soft Tympanostomy Tube

Otomedics Advanced Medical Technologies, Ltd., Kfar Saba, IL / Traditional, Substantially Equivalent

K071178 is the FDA 510(k) clearance record for OTOMEDICS SOFT TYMPANOSTOMY TUBE, a class II device, cleared for Otomedics Advanced Medical Technologies, Ltd. on under FDA product code ETD (Tube, Tympanostomy). FDA records list one 510(k) clearance for Otomedics Advanced Medical Technologies, Ltd. As of , FDA records show no recalls naming K071178.

Clearance record

Decision date
Received
(56 days to decision)
Product code
ETD Tube, Tympanostomy
Regulation
21 CFR 874.3880
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Otomedics Advanced Medical Technologies, Ltd. 20 Hata'As St., Kfar Saba, IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code ETD

Trailing 12 months
1 clearance under product code ETD in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code ETD, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260