510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K931717Substantially Equivalent

Yoshida/kaycor X-707 Wall Mounted Dental X-Ray

Kaycor Intl., Ltd., Northbrook IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K931717 is the FDA 510(k) clearance record for YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAY, a class II device, cleared for Kaycor Intl., Ltd. on under FDA product code EAP (Unit, X-Ray, Intraoral). FDA records list 7 510(k) clearances for Kaycor Intl., Ltd., from to . As of , FDA records show no recalls naming K931717.

Clearance record

Decision date
Received
(167 days to decision)
Product code
EAP Unit, X-Ray, Intraoral
Regulation
21 CFR 872.1810
Device class
Class II
Review panel
Dental
Applicant
Kaycor Intl., Ltd. 3611 Commercial Ave., Northbrook IL
510(k) summary
Statement
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