Manufacturer registered with FDA

Medipack Medical Packaging Mfg Co

DONGGUAN CITY, China. Lists 2 dental device types with FDA across 1 registered establishment.

FDA owner/operator9007710Contract manufacturerManufacturer
Device types listed
2
Brands and models
4
510(k) clearances
0as applicant
Markets registered in
520 registrations outside the US
Establishments
1China

Registered in 5 markets

Where regulators' registries name Medipack Medical Packaging Mfg Co as the manufacturer or the registration holder of a device.

All markets
United States: 2 device types listedEuropean Union: 11 registrationsTaiwan: 7 registrationsAustralia: 1 registrationsPeru: 1 registrations
RegisteredHome: ChinaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerMedipack Medical Packaging Mfg Co2 device types—Below
European UnionEUDAMEDManufacturerMedipack Medical Packaging Mfg. Co.11—Pure Global AI
TaiwanTFDAManufacturerMEDIPACK MEDICAL PACKAGING MFG CO.Medipack Medical Packaging Mfg Co.72005–2019Pure Global AI
AustraliaTGAManufacturerMedipack Medical Packaging Mfg Co12004–2004Pure Global AI
PeruDIGEMIDManufacturerMEDIPACK MEDICAL PACKAGING MFG. CO.12007–2007Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

Devices listed with FDA

What Medipack Medical Packaging Mfg Co currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Roll CottonEFN · Class 1—Maker—2009
Accessories Operative Dental UnitNRD · Class 1—Maker
UnigardUnigauzeUniguardUnipack
2011

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
MEDIPACK MEDICAL PACKAGING MFG. CO.FDA reg. 9680261DONGGUAN CITY Guangdong, ChinaContract manufacturer, Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9007710). 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.