Manufacturer registered with FDA

Rumex International Co.

Tampa, FL, United States. Lists 1 dental device type with FDA across 3 registered establishments.

FDA owner/operator9011770ManufacturerRepacker / relabeler
Device types listed
1
Brands and models
1
510(k) clearances
0as applicant
Markets registered in
13198 registrations outside the US
Establishments
3United Arab Emirates, Latvia, United States

Registered in 13 markets

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

All markets
United States: 1 device types listedSouth Korea: 59 registrationsSerbia: 46 registrationsCosta Rica: 27 registrationsPeru: 23 registrationsUnited Kingdom: 12 registrationsTaiwan: 10 registrationsBrazil: 7 registrationsAustralia: 6 registrationsColombia: 3 registrationsIsrael: 3 registrationsPhilippines: 1 registrationsSaudi Arabia: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerRumex International Co.1 device types—Below
South KoreaMFDSManufacturerRumex International Co.Rumex Baltics SIA · RUMEX INTERNATIONAL CO. · +2592008–2026Pure Global AI
SerbiaALIMSManufacturerRumex International Co.Rumex International Ltd.462025–2026Pure Global AI
Costa RicaMinisterio de SaludManufacturerRUMEX INTERNATIONAL CORumex International Ltd. · Rumex International, Ltd-27—Pure Global AI
PeruDIGEMIDManufacturerRUMEX INTERNATIONAL CO.232018–2026Pure Global AI
United KingdomMHRAManufacturerRumex International Ltd12—Pure Global AI
TaiwanTFDAManufacturerRUMEX INTERNATIONAL COMPANYRumex International Co · RUMEX International Company102006–2025Pure Global AI
BrazilANVISAManufacturerRUMEX INTERNATIONAL CO.72009–2024Pure Global AI
AustraliaTGAManufacturerRumex International Co62014–2014Pure Global AI
ColombiaINVIMAManufacturerRUMEX INTERNATIONAL CORUMEX INTERNATIONAL CO. · RUMEX INTERNATIONAL, CO3—Pure Global AI
IsraelAMARManufacturerRumex International CoRumex International Co. · Rumex International Company3—Pure Global AI
PhilippinesFDA PhilippinesManufacturerRumex International Ltd.12025–2025Pure Global AI
Saudi ArabiaSFDAManufacturerRumex International Ltd1—Pure 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 Rumex International Co. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Cartridge SyringeEJI · Class 2Dental needles & syringesMaker
RUMEX OPHTHALMIC INSTRUMENTS
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
Perfect Ophthalmic Instruments FZEFDA reg. 3031231776Dubai Dubayy, United Arab EmiratesManufacturer
RUMEX Baltics SIAFDA reg. 3012185136Riga, LatviaManufacturer
RUMEX INTERNATIONAL CO.FDA reg. 1058726Tampa, FL, United StatesRepacker / relabeler

Other names on FDA records

Rumex Baltics SIA · Perfect Ophthalmic Instruments FZE

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9011770). 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.