510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K213890Substantially Equivalent

IMICRYL Impression Materials

Imicryl Dis Malzemeleri San. ve Tic. A.S., Konya, TR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K213890 is the FDA 510(k) clearance record for IMICRYL Impression Materials, a class II device, cleared for Imicryl Dis Malzemeleri San. VE Tic. A.S. on under FDA product code ELW (Material, Impression). FDA records list one 510(k) clearance for Imicryl Dis Malzemeleri San. VE Tic. A.S. As of , FDA records show no recalls naming K213890.

Clearance record

Decision date
Received
(60 days to decision)
Product code
ELW Material, Impression
Regulation
21 CFR 872.3660
Device class
Class II
Review panel
Dental
Applicant
Imicryl Dis Malzemeleri San. VE Tic. A.S. Fetih Mahallesi Mahir Sokak No:5/201 Karatay, Konya, TR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code ELW

Trailing 12 months
3 clearances under product code ELW in the twelve months to October 2026, September 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code ELW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20262
October 20260