510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K811211Substantially Equivalent

Yoshida Ap 100

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

K811211 is the FDA 510(k) clearance record for YOSHIDA AP 100, a class II device, cleared for Kaycor Intl., Ltd. on under FDA product code EGY (Processor, Radiographic-Film, Automatic, Dental). FDA records list 7 510(k) clearances for Kaycor Intl., Ltd., from to . As of , FDA records show no recalls naming K811211.

Clearance record

Decision date
Received
(43 days to decision)
Product code
EGY Processor, Radiographic-Film, Automatic, Dental
Regulation
21 CFR 892.1900
Device class
Class II
Review panel
Radiology
Applicant
Kaycor Intl., Ltd. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EGY

Trailing 12 months

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

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