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Guilin Kevin Peter Technology Co., Ltd.: FDA-registered device maker in Guilin Guangxi, China, 4 510(k) clearances

Name: Guilin Kevin Peter Technology Co., Ltd. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Guilin Kevin Peter Technology Co., Ltd. is registered with the FDA (registration 3023816720) in Guilin Guangxi, China. It lists 16 device types. The FDA files 4 510(k) clearances under its listings, the newest dated September 18, 2026. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number: 3023816720
Address: North side of Linsu Rd, Lingui Town, Lingui Dist., Guilin, Guilin Guangxi, China, 541100
Owner or operator: Guilin Kevin Peter Technology Co., Ltd. (10085586)
Roles: Manufacturer
First device listed: July 6, 2022
Registered through: 2027
Brand names listed: 3D Printing Resin, Calcium Hydroxide Temporary Filling Material (KP-Cal ), DM Explore, DM Explore X, Dental Diode Laser Device(Laser-Pen, KP-Laser Pen), Disposable Sterile Root Canal File, EDTA Root Canal Lubricating Gel, EDTA Solution, Flowable Restorative Material(KP-Flow LF, KP-Flow MF, KP-Flow HF) and more

Devices it lists

Device	Product code	Class	Role	Source
Agent, Polishing, Abrasive, Oral Cavity	EJR	1	Manufacturer	accessdata.fda.gov
Dam, Rubber	EIE	1	Manufacturer	accessdata.fda.gov
File, Pulp Canal, Endodontic	EKS	1	Manufacturer	accessdata.fda.gov
Gutta-Percha	EKM	1	Manufacturer	accessdata.fda.gov
Light, Examination, Medical, Battery Powered	KYT	1	Manufacturer	accessdata.fda.gov
Liner, Cavity, Calcium Hydroxide	EJK	2	Manufacturer	accessdata.fda.gov
Loupe, Binocular, Low Power	HJH	1	Manufacturer	accessdata.fda.gov
Material, Impression Tray, Resin	EBH	1	Manufacturer	accessdata.fda.gov
Material, Tooth Shade, Resin	EBF	2	Manufacturer	accessdata.fda.gov
Microscope, Surgical	EPT	1	Manufacturer	accessdata.fda.gov
Powered Laser Surgical Instrument	GEX	2	Manufacturer	accessdata.fda.gov
Preparer, Root Canal Endodontic	EKQ	1	Manufacturer	accessdata.fda.gov
Resin, Root Canal Filling	KIF	2	Manufacturer	accessdata.fda.gov
Sealant, Pit And Fissure, And Conditioner	EBC	2	Manufacturer	accessdata.fda.gov
System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations	NOF	2	Manufacturer	accessdata.fda.gov
Unit, Operative Dental, Accessories	NRD	1	Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
September 18, 2026	K261047	Dental Diode Laser Device (Laser-Pen)	GEX	Substantially Equivalent	Guilin Kevin Peter Technology Co., Ltd.	accessdata.fda.gov
August 31, 2026	K261695	Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)	EBF	Substantially Equivalent	Guilin Kevin Peter Technology Co., Ltd.	accessdata.fda.gov
August 25, 2026	K261514	Calcium Hydroxide Temporary Filling Material (KP-Cal)	KIF	Substantially Equivalent	Guilin Kevin Peter Technology Co., Ltd.	accessdata.fda.gov
June 29, 2026	K261415	Injectable Root Canal Sealer (KP-Root SP)	KIF	Substantially Equivalent	Guilin Kevin Peter Technology Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated September 18, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.