510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K935689Substantially Equivalent

Ionosit Base Liner

Foremost Dental Mfg., Inc., Englewood NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935689 is the FDA 510(k) clearance record for IONOSIT BASE LINER, a class II device, cleared for Foremost Dental Mfg., Co. on under FDA product code EBD (Coating, Filling Material, Resin). FDA records list 15 510(k) clearances for Foremost Dental Mfg., Co., from to . As of , FDA records show no recalls naming K935689.

Clearance record

Decision date
Received
(53 days to decision)
Product code
EBD Coating, Filling Material, Resin
Regulation
21 CFR 872.3310
Device class
Class II
Review panel
Dental
Applicant
Foremost Dental Mfg., Co. 242 S. Dean St., Englewood NJ
510(k) summary
Summary
Third party review
No

Clearances, product code EBD

Trailing 12 months
1 clearance under product code EBD in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code EBD, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260