Data / Medical devices / Italy / Domino S.R.L.
Domino S.R.L.: FDA-registered device maker in Codogne Treviso, Italy, 5 510(k) clearances
Domino S.R.L. is registered with the FDA (registration 3006153348) in Codogne Treviso, Italy. It lists 9 device types. The FDA files 5 510(k) clearances under its listings, the newest dated November 7, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3006153348
- Address
- via Vittorio Veneto 52, Codogne Treviso, Italy, 31013
- Owner or operator
- DOMINO SRL (9090480)
- Roles
- Manufacturer
- First device listed
- August 1, 2006
- Registered through
- 2027
- Brand names listed
- Activa 700, Axon I Myo Pro, Bio Box Pro, Circuit Breaker, Cycling Pro, DX1000 PRO, DX500, Diacare 5500 Pro and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrode, Cutaneous | GXY | 2 | Manufacturer | accessdata.fda.gov |
| Exerciser, Powered | BXB | 1 | Manufacturer | accessdata.fda.gov |
| Interferential Current Therapy | LIH | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Vacuum, Radio Frequency Induced Heat | PBX | 2 | Manufacturer | accessdata.fda.gov |
| Platform, Force-Measuring | KHX | 1 | Manufacturer | accessdata.fda.gov |
| Stimulator, Muscle, Powered | IPF | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 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 |
|---|---|---|---|---|---|---|
| November 7, 2025 | K243131 | Triathlon Pro | NUH | Substantially Equivalent | Sigma Biomedical | accessdata.fda.gov |
| June 6, 2022 | K211207 | Diacare 7000 | PBX | Substantially Equivalent | Globus Sport and Health Technologies, LLC | accessdata.fda.gov |
| September 21, 2007 | K071431 | GLOBUS GENESY 1100 STIMULATOR | IPF | Substantially Equivalent | Domino S.R.L. | accessdata.fda.gov |
| April 30, 2007 | K061632 | GLOBUS PREMIUM MUSCLE STIMULATOR | NGX | Substantially Equivalent | Domino S.R.L. | accessdata.fda.gov |
| May 9, 1997 | K970426 | VALUETRODE | GXY | Substantially Equivalent | Axelgaard Mfg. Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Platform, Force-Measuring
- All makers of Massager, Vacuum, Radio Frequency Induced Heat
- All makers of Stimulator, Muscle, Powered, For Muscle Conditioning
- All makers of Electrode, Cutaneous
- All makers of Interferential Current Therapy
- All makers of Stimulator, Nerve, Transcutaneous, For Pain Relief
Updated November 7, 2025. 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.