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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

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

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 1-50 of 338

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  • Kp

    None Registry: GUDID Class:I

  • Kp

    None Registry: GUDID Class:I

  • Kp

    None Registry: GUDID Class:I

  • Kp-1708-19

    None Registry: GUDID Class:I

  • KP-16vt-21

    None Registry: GUDID Class:I

  • KP-16vt-25

    None Registry: GUDID Class:I

  • KP-16vt-31

    None Registry: GUDID Class:I

  • Kp-2504-21

    None Registry: GUDID Class:I

  • Kp-2504-25

    None Registry: GUDID Class:I

  • Kp-2004-31

    None Registry: GUDID Class:I

  • Kp-2004-25

    None Registry: GUDID Class:I

  • Kp-2004-21

    None Registry: GUDID Class:I

  • Kp-2504-31

    None Registry: GUDID Class:I

  • Kp-2506-21

    None Registry: GUDID Class:I

  • Kp-2506-25

    None Registry: GUDID Class:I

  • Kp-2506-31

    None Registry: GUDID Class:I

  • Kp-3004-21

    None Registry: GUDID Class:I

  • Kp-3004-25

    None Registry: GUDID Class:I

  • Kp-3504-25

    None Registry: GUDID Class:I

  • Kp-3504-21

    None Registry: GUDID Class:I

  • Kp-3504-31

    None Registry: GUDID Class:I

  • Kp-3004-31

    None Registry: GUDID Class:I

  • KP-12vt-25

    None Registry: GUDID Class:I

  • KP-12vt-21

    None Registry: GUDID Class:I

  • KP-12vt-31

    None Registry: GUDID Class:I

  • Kp-1704-21

    None Registry: GUDID Class:I

  • Kp-1506-21

    None Registry: GUDID Class:I

  • Kp-1805-25

    None Registry: GUDID Class:I

  • Kp-1805-21

    None Registry: GUDID Class:I

  • Kp-1704-25

    None Registry: GUDID Class:I

  • Kp-1506-25

    None Registry: GUDID Class:I

  • Kp-1704-31

    None Registry: GUDID Class:I

  • Kp-1506-31

    None Registry: GUDID Class:I

  • Kp-1805-31

    None Registry: GUDID Class:I

  • Kp-2006-21

    None Registry: GUDID Class:I

  • Kp-2006-25

    None Registry: GUDID Class:I

  • Kp-2006-31

    None Registry: GUDID Class:I

  • Kp-3006-21

    None Registry: GUDID Class:I

  • Kp-3006-25

    None Registry: GUDID Class:I

  • Kp-3506-21

    None Registry: GUDID Class:I

  • Kp-3006-31

    None Registry: GUDID Class:I

  • Kp-3506-31

    None Registry: GUDID Class:I

  • Kp-3506-25

    None Registry: GUDID Class:I

  • Kp-4004-21

    None Registry: GUDID Class:I

  • Kp-4004-25

    None Registry: GUDID Class:I

  • Kp

    None Registry: GUDID Class:I

  • Kp-4004-31

    None Registry: GUDID Class:I

  • Kp

    None Registry: GUDID Class:I

  • KP-12vt-21-T

    None Registry: GUDID Class:I

  • KP-12vt-25-T

    None Registry: GUDID Class:I

Rows 1-50 of 338

Showing 1-50 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

Frequently asked questions

How many devices does Guilin Kevin Peter Technology Co., Ltd. have in the registry?

The registry currently lists 338 devices for Guilin Kevin Peter Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Guilin Kevin Peter Technology Co., Ltd.'s devices?

Among its 50 most recently registered devices, Guilin Kevin Peter Technology Co., Ltd. has devices listed in FDA GUDID (50 devices).

What risk classes do Guilin Kevin Peter Technology Co., Ltd.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for Guilin Kevin Peter Technology Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Guilin Kevin Peter Technology Co., Ltd. in the registry?

The most recently registered devices listed for Guilin Kevin Peter Technology Co., Ltd. include KP, KP-1708-19, KP-16vt-21 and KP-16vt-25.

Which FDA establishments are linked to Guilin Kevin Peter Technology Co., Ltd.?

1 FDA establishment is linked to Guilin Kevin Peter Technology Co., Ltd. in the registry; they are listed on the company page.

Generated automatically from registry data and not verified by a human reviewer.