510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K060104Substantially Equivalent

Prismatik Clinical Zirconia

Glidewell Laboratories, Newport Beach CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K060104 is the FDA 510(k) clearance record for PRISMATIK CLINICAL ZIRCONIA, a class II device, cleared for Glidewell Laboratories on under FDA product code EIH (Powder, Porcelain). FDA records list 3 510(k) clearances for Glidewell Laboratories, from to . As of , FDA records show no recalls naming K060104.

Clearance record

Decision date
Received
(61 days to decision)
Product code
EIH Powder, Porcelain
Regulation
21 CFR 872.6660
Device class
Class II
Review panel
Dental
Applicant
Glidewell Laboratories 4141 Macarthur Blvd., Newport Beach CA
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