510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K881422Substantially Equivalent

Coe Pak Auto Mix, Regular or Hard Set

Coe Laboratories, Inc., Alsip IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K881422 is the FDA 510(k) clearance record for COE PAK AUTO MIX, REGULAR OR HARD SET, a class II device, cleared for Coe Laboratories, Inc. on under FDA product code EMA (Cement, Dental). FDA records list 20 510(k) clearances for Coe Laboratories, Inc., from to . As of , FDA records show no recalls naming K881422.

Clearance record

Decision date
Received
(209 days to decision)
Product code
EMA Cement, Dental
Regulation
21 CFR 872.3275
Device class
Class II
Review panel
Dental
Applicant
Coe Laboratories, Inc. 3737 W. 127th St., Alsip IL
Third party review
No

Clearances, product code EMA

Trailing 12 months
10 clearances under product code EMA in the twelve months to October 2026, December 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code EMA, trailing twelve months
MonthClearances
November 20250
December 20253
January 20260
February 20260
March 20261
April 20261
May 20261
June 20260
July 20261
August 20262
September 20261
October 20260