Manufacturer registered with FDA

S.G. Manufacturers

Sialkot, Pakistan. Lists 5 dental device types with FDA across 1 registered establishment.

FDA owner/operator10042485Manufacturer
Device types listed
5
Brands and models
5
510(k) clearances
0as applicant
Markets registered in
33 registrations outside the US
Establishments
1Pakistan

Registered in 3 markets

Where regulators' registries name S.G. Manufacturers as the manufacturer or the registration holder of a device.

All markets
United States: 5 device types listedTaiwan: 2 registrationsPeru: 1 registrations
RegisteredHome: PakistanOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerS.G. Manufacturers5 device types—Below
TaiwanTFDAManufacturerS. G. MANUFACTURERS22006–2006Pure Global AI
PeruDIGEMIDManufacturerSG MANUFACTURERS12023–2023Pure 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 S.G. Manufacturers currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Operative Amalgam CarrierEKI · Class 1Dental hand instrumentsMaker
CARRIER, AMALGAM, OPERATIVE
2018
Surgical Tooth Extractor ForcepsEMG · Class 1Dental hand instrumentsMaker
FORCEPS, TOOTH EXTRACTOR, SURGICAL
2018
Surgical Rongeur ForcepsEMH · Class 1Dental hand instrumentsMaker
FORCEPS, RONGEUR, SURGICAL
2018
Periodontic ScalerEMN · Class 1Dental hand instrumentsMaker
SCALER, PERIODONTIC
2018
Periodontic CuretteEMS · Class 1Dental hand instrumentsMaker
CURETTE, PERIODONTIC
2018

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
S.G. MANUFACTURERSFDA reg. 3002761766Sialkot Punjab, PakistanManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10042485). 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.