Guilin Kevin Peter Technology Co., Ltd. (manufacturer, Guilin Guangxi, CN): 7 new FDA device listings, incl. light, examination, medical, battery powered

Guilin Kevin Peter Technology Co., Ltd. (Guilin Guangxi): 7 new FDA device listings, incl. light, examination, medical, battery powered. Its amount of 7 is top-decile (90th percentile of 2,570 records). Dated 44 days ago, it serves as a historical benchmark. Score 85/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).

Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)

amount: 7 · 90th percentile of 2,570 DeviceEstablishmentPulse records · 7.0x the median

Free preview: all 14 published fields of this record are shown below. Locked: 499 related CN DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentGuilin Kevin Peter Technology Co., Ltd.
RoleManufacturer
Establishment typesManufacture Medical Device
LocationGuilin Guangxi, CN
New listings7
DevicesLight, Examination, Medical, Battery Powered; Material, Tooth Shade, Resin; Sealant, Pit And Fissure, And Conditioner; Resin, Root Canal Filling; Liner, Cavity, Calcium Hydroxide; Powered Laser Surgical Instrument
Product codesKYT, EBF, EBC, KIF, EJK, GEX
Device classesClass I, Class II
Medical specialtiesGeneral Hospital, Dental, General, Plastic Surgery
Brand namesSurgical Headlight; Flowable Restorative Material(KP-Flow LF, KP-Flow MF, KP-Flow HF); Injectable Root Canal Sealer (KP-Root SP); Calcium Hydroxide Temporary Filling Material (KP-Cal ); Dental Diode Laser Device(Laser-Pen, KP-Laser Pen)
First new listing2026-06-02
Latest new listing2026-09-22
FDA registration number3023816720
Registration expires2027-12-31
amount percentile90th of 2,570 (median 1, 7.0x median)
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL

  • Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
  • Record date: 2026-09-22
  • Data refreshed: 2026-10-28
  • Refunds on request within 14 days

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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT

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Peer benchmark and outreach value: Guilin Kevin Peter Technology Co., Ltd. and 687 CN peers

  • CN DeviceEstablishmentPulse records like this one: 687
  • Guilin Kevin Peter Technology Co., Ltd.'s amount: 90th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every CN peer: $137,400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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85 / 100 Score

  • Brings its own devices to market: buys manufacturing, sterilization and QMS help.
  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.
  • Listed in the last 45 days.

What is the DeviceEstablishmentPulse record for Guilin Kevin Peter Technology Co., Ltd. in Guilin Guangxi?

Guilin Kevin Peter Technology Co., Ltd. (Guilin Guangxi, CN), a manufacturer, added 7 FDA device listings between 2026-06-02 and 2026-09-22.

How does Guilin Kevin Peter Technology Co., Ltd. compare to other DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 7 is 7.0x the median of 1 across 2,570 records. It is 44 days old, still within a typical 45-day follow-up window. Its Score of 85/100 puts it among the stronger signals in this feed.

Guilin Kevin Peter Technology Co., Ltd. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Guilin Kevin Peter Technology Co., Ltd.Guilin Guangxi, CN790th2026-09-22
Abyrx, Inc.Stamford, CT790th2026-10-07
Boston Scientific Corp., Marina Bay Cust. Fulfillment CenterQuincy, MA688th2026-10-16
Inquis Medical, Inc.Menlo Park, CA587th2026-10-16

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✓ Read-only, live public data · Key and unlock right after payment · Card, Apple Pay, Google Pay or Link via Stripe · Refunds on request within 14 days

From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.

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