Manufacturer registered with FDA

Improve Co.,limited

Lantau Island, Hong Kong SAR China. Lists 8 dental device types with FDA across 1 registered establishment.

FDA owner/operator10060190Contract manufacturerForeign exporterManufacturer
Device types listed
8
Brands and models
18
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1China

Devices listed with FDA

What Improve Co.,limited currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Resin Impression Tray MaterialEBH · Class 1Impression traysMaker
dental models
2023
Orthodontic SpringECO · Class 1Orthodontic wires & bandsMaker
Clear aligner
2025
Orthodontic Metal BracketEJF · Class 1Orthodontic bracketsMaker
BRACKET, METAL, ORTHODONTICMetal partial framework (CoCr metal Partial , for Dental Restoration, Finished Product, Unused)
2019
Posterior with Metal Insert Artificial TeethELJ · Class 1—Maker
arylic dentureE.max crown/bridgeE.max crown/bridge, Valplastmetal framework denturePorcelain fused to metal crown/bridgePorcelain fused to metalcrown/bridges, zirconia crown/bridges, metal framework dentures, arylic denturesValplastzirconia crown/bridge
2019
Backing and Facing Artificial TeethELK · Class 1—Maker
TEETH, ARTIFICIAL, BACKING AND FACING
2019
Teeth Plastic DentureELM · Class 2Denture resins & teethMaker
arylic dentures
2025
Preformed CrownELZ · Class 1—Maker
CROWN, PREFORMEDPlaster Models Including mixed MaterialPorcelain fused to metal crown/bridges, zirconia crown/bridges, E.max crownbridge
2019
Endosseous Dental Implant AccessoriesNDP · Class 1Implant instruments & surgical kitsMaker
Accessories, implant, dental,
2019

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
IMPROVE CO.,LIMITEDFDA reg. 3014253211Lantau Island Hong Kong, ChinaContract manufacturer, Foreign exporter, Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10060190). 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.