Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K030607Substantially Equivalent

Kavo Everest G-Blank, Kavo Everest G-Ceram, Coating Ceramic Lf-3-Pfm, Glaze and Colorings/staining/shades

Kavo America, Lake Zurich IL / Traditional, Substantially Equivalent

K030607 is the FDA 510(k) clearance record for KAVO EVEREST G-BLANK, KAVO EVEREST G-CERAM, COATING CERAMIC LF-3-PFM, GLAZE AND COLORINGS/STAINING/SHADES, a class II device, cleared for Kavo America on under FDA product code EIH (Powder, Porcelain). FDA records list 24 510(k) clearances for Kavo America, from to . As of , FDA records show no recalls naming K030607.

Clearance record

Decision date
Received
(65 days to decision)
Product code
EIH Powder, Porcelain
Regulation
21 CFR 872.6660
Device class
Class II
Review panel
Dental
Applicant
Kavo America 340 E. Main St., Lake Zurich IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code EIH

Trailing 12 months
13 clearances under product code EIH in the twelve months to October 2026, June 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code EIH, trailing twelve months
MonthClearances
November 20250
December 20251
January 20262
February 20260
March 20262
April 20261
May 20261
June 20263
July 20262
August 20261
September 20260
October 20260