# Guilin Kevin Peter Technology Co., Ltd. (manufacturer, Guilin Guangxi, CN): 7 new FDA device listings, incl. material, tooth shade, resin

**Score:** 85/100

| Field | Value |
|---|---|
| Establishment | Guilin Kevin Peter Technology Co., Ltd. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Guilin Guangxi, CN |
| New listings | 7 |
| Devices | Material, Tooth Shade, Resin; Sealant, Pit And Fissure, And Conditioner; Powered Laser Surgical Instrument; Light, Examination, Medical, Battery Powered; Resin, Root Canal Filling; Liner, Cavity, Calcium Hydroxide |
| Product codes | EBF, EBC, GEX, KYT, KIF, EJK |
| Device classes | Class I, Class II |
| Medical specialties | Dental, General, Plastic Surgery, General Hospital |
| Brand names | Flowable Restorative Material(KP-Flow LF, KP-Flow MF, KP-Flow HF); Dental Diode Laser Device(Laser-Pen, KP-Laser Pen); Surgical Headlight; Injectable Root Canal Sealer (KP-Root SP); Calcium Hydroxide Temporary Filling Material (KP-Cal ) |
| First new listing | 2026-06-02 |
| Latest new listing | 2026-09-22 |
| FDA registration number | 3023816720 |
| Registration expires | 2027-12-31 |

## Why this 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.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-11-04T21:52:36.524Z.
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.