510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K100248Substantially Equivalent

Drfp Prosmart Root Canal Obturation System, Propoints 4% 6%, Pt, S

Drfp, Ltd., Amsterdam, Nh, NL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K100248 is the FDA 510(k) clearance record for DRFP PROSMART ROOT CANAL OBTURATION SYSTEM, PROPOINTS 4% 6%, PT, S, a class II device, cleared for Drfp , Ltd. on under FDA product code KIF (Resin, Root Canal Filling). FDA records list one 510(k) clearance for Drfp , Ltd. As of , FDA records show no recalls naming K100248.

Clearance record

Decision date
Received
(268 days to decision)
Product code
KIF Resin, Root Canal Filling
Regulation
21 CFR 872.3820
Device class
Class II
Review panel
Dental
Applicant
Drfp , Ltd. Amstel 320-I, Amsterdam, Nh, NL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KIF

Trailing 12 months
6 clearances under product code KIF in the twelve months to October 2026, January 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code KIF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20262
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20261
September 20262
October 20260