510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K897143Substantially Equivalent

Vera 103

Madsen North America, Inc., North Tonawanda NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K897143 is the FDA 510(k) clearance record for VERA 103, a class II device, cleared for Madsen North America, Inc. on under FDA product code LYN (Apparatus, Visual Reinforcement Audiometric). FDA records list 3 510(k) clearances for Madsen North America, Inc., from to . As of , FDA records show no recalls naming K897143.

Clearance record

Decision date
Received
(121 days to decision)
Product code
LYN Apparatus, Visual Reinforcement Audiometric
Regulation
21 CFR 874.1050
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Madsen North America, Inc. 908 Niagara Falls Blvd., North Tonawanda NY
Third party review
No

Clearances, product code LYN

Trailing 12 months

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

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