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FDA 510(k)

Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)

K-Number: K261695 · 2026-08-31

ApplicantGuilin Kevin Peter Technology Co., Ltd.
Decision Date2026-08-31
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF) is the device name listed in this FDA 510(k) record. The listed applicant is Guilin Kevin Peter Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-08-31 under 510(k) number K261695. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)?

Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF) is a medical device that received FDA 510(k) clearance on 2026-08-31. The listed applicant is Guilin Kevin Peter Technology Co., Ltd.. The 510(k) number is K261695.

When did Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF) receive FDA 510(k) clearance?

Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF) received FDA 510(k) clearance on 2026-08-31, under 510(k) number K261695.

Who is the listed applicant for Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)?

The FDA 510(k) record lists Guilin Kevin Peter Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)?

The FDA product code for Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF) is EBF.

Other records listing Guilin Kevin Peter Technology Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261514Calcium Hydroxide Temporary Filling Material (KP-Cal)K261415Injectable Root Canal Sealer (KP-Root SP)

Related Devices (Code: EBF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K261246SRGC-06GC America, Inc.K261093DIAFILDiaDent Group InternationalK261071DIAFIL Bulk FLOW (Economic Package);DIAFIL Bulk FLOW (Refill Package);DIAFIL Bulk FLOW (0.5g)DiaDent Group InternationalK260805Dual CoreVericom Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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