Data / Medical devices / Czechia / ADM, a.s.
ADM, a.s.: FDA-registered device maker in Brno Mesto Brno, Czechia, 1 510(k) clearance
ADM, a.s. is registered with the FDA (registration 3005347791) in Brno Mesto Brno, Czechia. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 10, 1995. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3005347791
- Address
- U Vodarny 2, Brno Mesto Brno, Czechia, 61600
- Owner or operator
- ADM, a.s. (9077377)
- Roles
- Manufacturer
- First device listed
- September 12, 2005
- Registered through
- 2026
- Brand names listed
- DENTAPREG, Dentapreg BRAID, Dentapreg BUNDLE, Dentapreg INTRO, Dentapreg MESH, Dentapreg MESH Economy Pack, Dentapreg PFM, Dentapreg PFU and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Material, Tooth Shade, Resin | EBF | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 10, 1995 | K952353 | EZ-COMP | EBF | Substantially Equivalent | Adm, Inc. | accessdata.fda.gov |
Compare with other makers
Updated August 10, 1995. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.