Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K081263Substantially Equivalent

Starceram

H.C. Starck Ceramics GmbH & Co.Kg, Golden CO / Abbreviated, Substantially Equivalent

K081263 is the FDA 510(k) clearance record for STARCERAM, a class II device, cleared for H.C. Starck Ceramics GmbH & Co.Kg on under FDA product code EIH (Powder, Porcelain). FDA records list one 510(k) clearance for H.C. Starck Ceramics GmbH & Co.Kg. As of , FDA records show no recalls naming K081263.

Clearance record

Decision date
Received
(57 days to decision)
Product code
EIH Powder, Porcelain
Regulation
21 CFR 872.6660
Device class
Class II
Review panel
Dental
Applicant
H.C. Starck Ceramics GmbH & Co.Kg 13605 W. 7th Ave., Golden CO
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