510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K832065Substantially Equivalent

Acuracy 071, Dental, Intraoral-X-Ray

Belmont Equipment Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K832065 is the FDA 510(k) clearance record for ACURACY 071, DENTAL, INTRAORAL-X-RAY, a class II device, cleared for Belmont Equipment Corp. on under FDA product code EAP (Unit, X-Ray, Intraoral). FDA records list 12 510(k) clearances for Belmont Equipment Corp., from to . As of , FDA records show no recalls naming K832065.

Clearance record

Decision date
Received
(77 days to decision)
Product code
EAP Unit, X-Ray, Intraoral
Regulation
21 CFR 872.1810
Device class
Class II
Review panel
Dental
Applicant
Belmont Equipment Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EAP

Trailing 12 months

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

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