Medical Device
Manufacturing
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K230487Substantially Equivalent

Dental Lithium Disilicate Glass-Ceramic

Fuzhou Rick Brown Biomaterials Co. Ltd., Fuzhou, CN / Traditional, Substantially Equivalent

K230487 is the FDA 510(k) clearance record for Dental Lithium Disilicate Glass-Ceramic, a class II device, cleared for Fuzhou Rick Brown Biomaterials Co., Ltd. on under FDA product code EIH (Powder, Porcelain). FDA records list one 510(k) clearance for Fuzhou Rick Brown Biomaterials Co., Ltd. As of , FDA records show no recalls naming K230487.

Clearance record

Decision date
Received
(130 days to decision)
Product code
EIH Powder, Porcelain
Regulation
21 CFR 872.6660
Device class
Class II
Review panel
Dental
Applicant
Fuzhou Rick Brown Biomaterials Co., Ltd. The First And Second Floors Of R&D Bldg., Jiecheng, Fuzhou, CN
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