Registered with FDA

Saferlife Products Co.,Ltd.

Guangzhou, China. Lists 1 dental device type with FDA across 1 registered establishment.

FDA owner/operator10031800Repacker / relabeler
Device types listed
1
Brands and models
2
510(k) clearances
0as applicant
Markets registered in
410 registrations outside the US
Establishments
1China

Registered in 4 markets

Where regulators' registries name Saferlife Products Co.,Ltd. as the manufacturer or the registration holder of a device.

All markets
United States: 1 device types listedSouth Korea: 5 registrationsTaiwan: 3 registrationsAustralia: 2 registrations
RegisteredHome: ChinaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAListerSaferlife Products Co.,Ltd.1 device types—Below
South KoreaMFDSManufacturerSAFERLIFE PRODUCTS CO.,LIMITEDSAFERLIFE PRODUCTS CO., LIMITED · SAFERLIFE PRODUCTS CO.,LTD · +152018–2023Pure Global AI
TaiwanTFDAManufacturerSaferlife Products Co., Ltd.SAFERLIFE PRODUCTS CO., LTD.32016–2023Pure Global AI
AustraliaTGAManufacturerSaferlife Products Co Limited22011–2020Pure 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 Saferlife Products Co.,Ltd. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Suction Operatory UnitEBR · Class 1Suction & evacuation unitsLister
Suction pumpSuction unit
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
SAFERLIFE PRODUCTS CO.,LTD.FDA reg. 3008264111Guangzhou Guangdong, ChinaRepacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10031800). 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.