510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K261415Substantially Equivalent

Injectable Root Canal Sealer (KP-Root SP)

Guilin Kevin Peter Technology Co., Ltd., Guilin, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K261415 is the FDA 510(k) clearance record for Injectable Root Canal Sealer (KP-Root SP), a class II device, cleared for Guilin Kevin Peter Technology Co., Ltd. on under FDA product code KIF (Resin, Root Canal Filling). FDA records list one 510(k) clearance for Guilin Kevin Peter Technology Co., Ltd. As of , FDA records show no recalls naming K261415.

Clearance record

Decision date
Received
(60 days to decision)
Product code
KIF Resin, Root Canal Filling
Regulation
21 CFR 872.3820
Device class
Class II
Review panel
Dental
Applicant
Guilin Kevin Peter Technology Co., Ltd. North Side Of Linsu Rd., Lingui Town, Lingui Dist., Guilin, CN
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