510(K) CLEARANCES 49 ▼18RECALLS POSTED 23 ▼3CLASS I 1 ▼1PMA DECISIONS 37 ▼3WEEK ENDING / FDA DATA AS OF
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K900393Substantially Equivalent

Opaque Porcelain

Dentsply Intl., York PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900393 is the FDA 510(k) clearance record for OPAQUE PORCELAIN, a class II device, cleared for Dentsply Intl. on under FDA product code EIH (Powder, Porcelain). FDA records list 291 510(k) clearances for Dentsply Intl., from to . As of , FDA records show no recalls naming K900393.

Clearance record

Decision date
Received
(77 days to decision)
Product code
EIH Powder, Porcelain
Regulation
21 CFR 872.6660
Device class
Class II
Review panel
Dental
Applicant
Dentsply Intl. 570 W. College Ave., York PA
Third party review
No

Clearances, product code EIH

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