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
K030699Substantially Equivalent

Veraviewepocs Panoramic/cephalometric X-Ray Unit with Cephalometric

J. Morita Mfg. Corp., Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K030699 is the FDA 510(k) clearance record for VERAVIEWEPOCS PANORAMIC/CEPHALOMETRIC X-RAY UNIT WITH CEPHALOMETRIC, a class II device, cleared for J. Morita Mfg. Corp. on under FDA product code EAG (Cephalometer). FDA records list one 510(k) clearance for J. Morita Mfg. Corp. As of , FDA records show no recalls naming K030699.

Clearance record

Decision date
Received
(84 days to decision)
Product code
EAG Cephalometer
Regulation
21 CFR 872.1830
Device class
Class II
Review panel
Dental
Applicant
J. Morita Mfg. Corp. 1425 K St. NW, Washington DC
510(k) summary
Summary PDF
Third party review
No

Clearances, product code EAG

Trailing 12 months

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

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