Manufacturer registered with FDA
MICROMA Martin Alber GmbH & Co. KG
IRNDORF, Germany. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 0
- 510(k) clearances
- 0as applicant
- Markets registered in
- 62,607 registrations outside the US
- Establishments
- 1Germany
Registered in 6 markets
Where regulators' registries name MICROMA Martin Alber GmbH & Co. KG as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Manufacturer | MICROMA Martin Alber GmbH & Co. KG | 1 device types | — | Below |
| Thailand | Thai FDA | Manufacturer | MICROMA MARTIN ALBER GMBH & CO. KG | 2,590 | — | Pure Global AI |
| Brazil | ANVISA | Manufacturer | MICROMA MARTIN ALBER GMBH & CO. KG | 6 | 2026–2026 | Pure Global AI |
| South Korea | MFDS | Manufacturer | MICROMA Martin Alber GmbH & Co. KG | 5 | 2014–2024 | Pure Global AI |
| Taiwan | TFDA | Manufacturer | MICROMA MARTIN ALBER GMBH & CO. KG | 5 | 2006–2017 | Pure Global AI |
| Colombia | INVIMA | Manufacturer | MICROMA MARTIN ALBER GMBH & CO. KG | 1 | — | 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 MICROMA Martin Alber GmbH & Co. KG currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| All Types RetractorEIG · Class 1 | Dental hand instruments | Maker | — | 1992 |
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
| Establishment | Location | What it does |
|---|---|---|
| MICROMA MARTIN ALBER GMBH & CO. KGFDA reg. 8043895 | IRNDORF Baden-Wurttemberg, Germany | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9004373). 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.