Manufacturer registered with FDA

Crimson International

Sialkot, Pakistan. Lists 2 dental device types with FDA across 1 registered establishment.

FDA owner/operator10062421Manufacturer
Device types listed
2
Brands and models
2
510(k) clearances
0as applicant
Markets registered in
387 registrations outside the US
Establishments
1Pakistan

Registered in 3 markets

Where regulators' registries name Crimson International as the manufacturer or the registration holder of a device.

All markets
United States: 2 device types listedEuropean Union: 86 registrationsTaiwan: 1 registrations
RegisteredHome: PakistanOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerCrimson International2 device types—Below
European UnionEUDAMEDManufacturerCrimson International86—Pure Global AI
TaiwanTFDAManufacturerCRIMSON International12019–2019Pure 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 Crimson International currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Rubber Dam Clamp ForcepsEJG · Class 1Rubber dam systemsMaker
FORCEPS, RUBBER DAM CLAMP
2022
Surgical Tooth Extractor ForcepsEMG · Class 1Dental hand instrumentsMaker
FORCEPS, TOOTH EXTRACTOR, SURGICAL
2020

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
CRIMSON INTERNATIONALFDA reg. 3015143057Sialkot Punjab, PakistanManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10062421). 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.