510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K060860Substantially Equivalent

Turkom-Cera

Dental Suppliers of America, Inc., Arlington WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K060860 is the FDA 510(k) clearance record for TURKOM-CERA, a class II device, cleared for Dental Suppliers of America, Inc. on under FDA product code EIH (Powder, Porcelain). FDA records list one 510(k) clearance for Dental Suppliers of America, Inc. As of , FDA records show no recalls naming K060860.

Clearance record

Decision date
Received
(51 days to decision)
Product code
EIH Powder, Porcelain
Regulation
21 CFR 872.6660
Device class
Class II
Review panel
Dental
Applicant
Dental Suppliers of America, Inc. 18616 123rd. Ave. NE, Arlington WA
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