Manufacturer registered with FDA

CPM Precision GmbH

Hirschberg, Germany. Lists 3 dental device types with FDA across 1 registered establishment.

FDA owner/operator10062608Contract manufacturer
Device types listed
3
Brands and models
0
510(k) clearances
0as applicant
Markets registered in
39 registrations outside the US
Establishments
1Germany

Registered in 3 markets

Where regulators' registries name CPM Precision GmbH as the manufacturer or the registration holder of a device.

All markets
United States: 3 device types listedSouth Korea: 5 registrationsTaiwan: 4 registrations
RegisteredHome: GermanyOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerCPM Precision GmbH3 device types—Below
South KoreaMFDSManufacturerCPM Precision GmbHCPM Precision GmBH · CPM Precision GmbH.52011–2021Pure Global AI
TaiwanTFDAManufacturerCPM Precision GmbH42011–2023Pure 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 CPM Precision GmbH currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Root-Form Endosseous ImplantDZE · Class 2Dental implantsMaker—2024
Endosseous Dental Implant AccessoriesNDP · Class 1Implant instruments & surgical kitsMaker—2020
Endosseous Dental Implant AbutmentNHA · Class 2Implant abutmentsMaker—2024

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
CPM PRECISION GMBHFDA reg. 3015160953Hirschberg Baden-Wurttemberg, GermanyContract manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10062608). 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.