510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K932426Substantially Equivalent

Beltone Opera/opera Mhp/opera Max

Beltone Electronics Corp., Chicago IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K932426 is the FDA 510(k) clearance record for BELTONE OPERA/OPERA MHP/OPERA MAX, a class I device, cleared for Beltone Electronics Corp. on under FDA product code ESD (Hearing Aid, Air-Conduction, Prescription). FDA's definition for product code ESD reads: "An air-conduction hearing aid is a wearable sound amplifying device intended to compensate for impaired hearing that conducts sound to the ear through the air. This is a prescription hearing aid". FDA records list 42 510(k) clearances for Beltone Electronics Corp., from to . As of , FDA records show no recalls naming K932426.

Clearance record

Decision date
Received
(56 days to decision)
Product code
ESD Hearing Aid, Air-Conduction, Prescription
Regulation
21 CFR 874.3300
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Beltone Electronics Corp. 4201 W. Victoria St., Chicago IL
510(k) summary
Summary
Third party review
No

Clearances, product code ESD

Trailing 12 months

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

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