510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K000154Substantially Equivalent

Eliachar Laryngeal Foam Stent, Model Ell-1

E. Benson Hood Lab, Inc., Pembroke MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K000154 is the FDA 510(k) clearance record for ELIACHAR LARYNGEAL FOAM STENT, MODEL ELL-1, a class II device, cleared for E. Benson Hood Lab, Inc. on under FDA product code FWN (Prosthesis, Larynx (Stents And Keels)). FDA records list 3 510(k) clearances for E. Benson Hood Lab, Inc., from to . As of , FDA records show no recalls naming K000154.

Clearance record

Decision date
Received
(70 days to decision)
Product code
FWN Prosthesis, Larynx (Stents And Keels)
Regulation
21 CFR 874.3620
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
E. Benson Hood Lab, Inc. 575 Washington St., Pembroke MA
510(k) summary
Summary
Third party review
No

Clearances, product code FWN

Trailing 12 months

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

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