510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K965072Substantially Equivalent

Panoura Ultra Pan and Panoura Ultra Pan/ceph Panoramic/cephalometric X-Ray Unit

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

K965072 is the FDA 510(k) clearance record for PANOURA ULTRA PAN AND PANOURA ULTRA PAN/CEPH PANORAMIC/CEPHALOMETRIC X-RAY UNIT, a class II device, cleared for Kaycor Intl., Ltd. on under FDA product code EHD (Unit, X-Ray, Extraoral With Timer). FDA records list 7 510(k) clearances for Kaycor Intl., Ltd., from to . As of , FDA records show no recalls naming K965072.

Clearance record

Decision date
Received
(39 days to decision)
Product code
EHD Unit, X-Ray, Extraoral With Timer
Regulation
21 CFR 872.1800
Device class
Class II
Review panel
Dental
Applicant
Kaycor Intl., Ltd. 3611 Commercial Ave., Northbrook IL
510(k) summary
Summary
Third party review
No

Clearances, product code EHD

Trailing 12 months
6 clearances under product code EHD in the twelve months to October 2026, February 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code EHD, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20262
March 20262
April 20260
May 20261
June 20260
July 20260
August 20260
September 20261
October 20260