Manufacturer registered with FDA

Elite Dental Lab

Huizhou City, China. Lists 15 dental device types with FDA across 1 registered establishment.

FDA owner/operator10086289Manufacturer
Device types listed
15
Brands and models
18
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1China

Devices listed with FDA

What Elite Dental Lab currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Dental Hand InstrumentsDZN · Class 1Dental hand instrumentsMaker
Dental ForcepsModel Trimmer ToolsPlaster Knife
2026
Mouth MirrorEAX · Class 1Dental hand instrumentsMaker
Mouth Mirror
2026
Resin Impression Tray MaterialEBH · Class 1Impression traysMaker
Artificial Gingiva Materials
2026
Rubber Dam ClampEEF · Class 1Rubber dam systemsMaker
Rubber Dam Clamp
2026
Dental Dressing ForcepsEFL · Class 1Dental hand instrumentsMaker
Cotton Pliers
2026
Preformed Impression TrayEHY · Class 1Impression traysMaker
Preformed Impression Tray
2026
Restorative and Impression Material SyringeEID · Class 1Dental hand instrumentsMaker
silicone impression
2026
Rubber DamEIE · Class 1Rubber dam systemsMaker
Rubber Dam
2026
Dental Wax CarverEIK · Class 1Dental hand instrumentsMaker
Wax Carver
2026
Periodontic ProbeEIX · Class 1Dental hand instrumentsMaker
Periodontal Probe
2026
Dental Plastic Filling InstrumentEIY · Class 1Dental hand instrumentsMaker
Composite Filling InstrumentDental Composite Sculpting Instrument
2026
Rubber Dam FrameEJE · Class 1Rubber dam systemsMaker
Rubber Dam Frame
2026
Rubber Dam Clamp ForcepsEJG · Class 1Rubber dam systemsMaker
Rubber Dam Forceps
2026
Operative ExplorerEKB · Class 1Dental hand instrumentsMaker
Dental Explorer
2026
Resin ApplicatorKXR · Class 1—Maker
Resin Applicator
2026

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

Registered establishments

EstablishmentLocationWhat it does
ELITE DENTAL LABFDA reg. 3024946194Huizhou City Guangdong, ChinaManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10086289). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.