510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K863816Substantially Equivalent

Ivory Premium Rubber Dam

Columbus Dental Mfg. Co., St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K863816 is the FDA 510(k) clearance record for IVORY PREMIUM RUBBER DAM, a class I device, cleared for Columbus Dental Mfg. Co. on under FDA product code EIE (Dam, Rubber). FDA records list 11 510(k) clearances for Columbus Dental Mfg. Co., from to . As of , FDA records show no recalls naming K863816.

Clearance record

Decision date
Received
(27 days to decision)
Product code
EIE Dam, Rubber
Regulation
21 CFR 872.6300
Device class
Class I
Review panel
Dental
Applicant
Columbus Dental Mfg. Co. 1000 Chouteau Ave., St. Louis MO
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