Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K842844Substantially Equivalent

Denti-D Rubber Dam

Fema Corp., Mchenry IL / Traditional, Substantially Equivalent

K842844 is the FDA 510(k) clearance record for DENTI-D RUBBER DAM, a class I device, cleared for Fema Corp. on under FDA product code EIE (Dam, Rubber). FDA records list one 510(k) clearance for Fema Corp. As of , FDA records show no recalls naming K842844.

Clearance record

Decision date
Received
(28 days to decision)
Product code
EIE Dam, Rubber
Regulation
21 CFR 872.6300
Device class
Class I
Review panel
Dental
Applicant
Fema Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EIE

Trailing 12 months

FDA records hold no clearances under product code EIE in the trailing twelve months.

FDA records show no clearances under product code EIE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EIE, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260