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Guilin Kevin Peter Technology Co., Ltd.

Country not established FDA

Part of Guilin Kevin Peter Technology Co., Ltd.

Devices
338
Registrations
FDA
FDA recalls
0

What Guilin Kevin Peter Technology Co., Ltd. makes

Guilin Kevin Peter Technology Co., Ltd. manufactures reusable rotary and reciprocating endodontic files, designed for root canal preparation, as well as natural gutta-percha for root canal filling procedures.

The company’s products are classified as Class I medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States.

AI-generated from registry data, 19 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue338

Newest first, rows 101-150 of 338

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  • Dm Kp-2004-25

    None Registry: GUDID Class:I

  • Dm Kp-2504-21

    None Registry: GUDID Class:I

  • Dm Kp-2004-31

    None Registry: GUDID Class:I

  • Dm Kp-2504-25

    None Registry: GUDID Class:I

  • Dm Kp-2506-21

    None Registry: GUDID Class:I

  • Dm Kp-2504-31

    None Registry: GUDID Class:I

  • Dm Kp-2506-25

    None Registry: GUDID Class:I

  • Dm Kp-2506-31

    None Registry: GUDID Class:I

  • DM KP-12vt-21

    None Registry: GUDID Class:I

  • DM KP-12vt-31

    None Registry: GUDID Class:I

  • DM KP-12vt-25

    None Registry: GUDID Class:I

  • Dm Kp-1302-21

    None Registry: GUDID Class:I

  • Dm Kp-1302-31

    None Registry: GUDID Class:I

  • Dm Kp-1302-25

    None Registry: GUDID Class:I

  • Dm Kp-1506-21

    None Registry: GUDID Class:I

  • Dm Kp-1506-25

    None Registry: GUDID Class:I

  • Dm Kp-1506-31

    None Registry: GUDID Class:I

  • Dm Kp-1602-31

    None Registry: GUDID Class:I

  • Dm Kp-1602-21

    None Registry: GUDID Class:I

  • Dm Kp-1602-25

    None Registry: GUDID Class:I

  • Dm Kp-1704-21

    None Registry: GUDID Class:I

  • Dm Kp-1704-25

    None Registry: GUDID Class:I

  • Dm Kp-1704-31

    None Registry: GUDID Class:I

  • Dm Kp-1902-21

    None Registry: GUDID Class:I

  • Dm Kp-1902-25

    None Registry: GUDID Class:I

  • Dm Kp-3006-21

    None Registry: GUDID Class:I

  • Dm Kp-3004-25

    None Registry: GUDID Class:I

  • Dm Kp-3004-21

    None Registry: GUDID Class:I

  • Dm Kp-2006-31

    None Registry: GUDID Class:I

  • Dm Kp-3004-31

    None Registry: GUDID Class:I

  • Dm Kp-2006-21

    None Registry: GUDID Class:I

  • Dm Kp-2006-25

    None Registry: GUDID Class:I

  • Dm Kp-1902-31

    None Registry: GUDID Class:I

  • Dm Kp-3006-25

    None Registry: GUDID Class:I

  • Dm Kp-3504-21

    None Registry: GUDID Class:I

  • Dm Kp-3006-31

    None Registry: GUDID Class:I

  • Dm Kp-3504-25

    None Registry: GUDID Class:I

  • Dm Kp-3504-31

    None Registry: GUDID Class:I

  • Dm Kp-3506-21

    None Registry: GUDID Class:I

  • Dm Kp-3506-25

    None Registry: GUDID Class:I

  • Dm Kp-3506-31

    None Registry: GUDID Class:I

  • Dm Kp-4004-21

    None Registry: GUDID Class:I

  • Dm Kp-4004-25

    None Registry: GUDID Class:I

  • Dm Kp-5004-21

    None Registry: GUDID Class:I

  • Dm Kp-4004-31

    None Registry: GUDID Class:I

  • Dm Kp-5004-25

    None Registry: GUDID Class:I

  • Dm Kp-5004-31

    None Registry: GUDID Class:I

  • Dm

    None Registry: GUDID Class:I

  • Dm

    None Registry: GUDID Class:I

  • Dm

    None Registry: GUDID Class:I

Rows 101-150 of 338

Showing 101-150 of 338

Company details

DUNS number
621948840

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Guilin Kevin Peter Technology Co., Ltd. Guilin Guangxi · CN FEI 3023816720