Registered with FDA

Medica Corporation

Bedford, MA, United States. Lists 1 dental device type with FDA across 1 registered establishment.

FDA owner/operator1220972Repacker / relabeler
Device types listed
1
Brands and models
1
510(k) clearances
0as applicant
Markets registered in
6115 registrations outside the US
Establishments
1United States

Registered in 6 markets

Where regulators' registries name Medica Corporation as the manufacturer or the registration holder of a device.

All markets
United States: 1 device types listedTaiwan: 59 registrationsBrazil: 30 registrationsColombia: 16 registrationsPeru: 9 registrationsIsrael: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAListerMedica Corporation1 device types—Below
TaiwanTFDAManufacturerMEDICA CORPORATION592005–2024Pure Global AI
BrazilANVISAManufacturerMEDICA CORPORATION302010–2025Pure Global AI
ColombiaINVIMAManufacturerMEDICA CORP.MEDICA CORPORATION16—Pure Global AI
PeruDIGEMIDManufacturerMEDICA CORPORATIONMEDICA CORP.92015–2024Pure Global AI
IsraelAMARManufacturerMedica Corporation1—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 Medica Corporation currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Intraosseous Fixation WireDZK · Class 2—Lister
Amphetamines (AMP)
2013

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
MEDICA CORP.FDA reg. 1220972BEDFORD, MA, United StatesRepacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 1220972). 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.