Data / Medical devices / Italy / Inventis SRL
Inventis SRL: FDA-registered device maker in Padova, Italy, 2 510(k) clearances
Inventis SRL is registered with the FDA (registration 3008699634) in Padova, Italy. It lists 8 device types. The FDA files 2 510(k) clearances under its listings, the newest dated January 3, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3008699634
- Address
- Via Austria, 38, Padova, Italy, 35127
- Owner or operator
- Inventis srl (10033997)
- Roles
- Manufacturer
- First device listed
- October 26, 2010
- Registered through
- 2027
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Audiometer | EWO | 2 | Manufacturer | accessdata.fda.gov |
| Calibrator, Hearing Aid / Earphone And Analysis Systems | ETW | 2 | Manufacturer | accessdata.fda.gov |
| Camera, Television, Endoscopic, With Audio | FWG | 1 | Manufacturer | accessdata.fda.gov |
| Laryngostroboscope | EQL | 1 | Manufacturer | accessdata.fda.gov |
| Medical Device Data System | OUG | 1 | Manufacturer | accessdata.fda.gov |
| Nystagmograph | GWN | 2 | Manufacturer | accessdata.fda.gov |
| Otoscope | ERA | 1 | Manufacturer | accessdata.fda.gov |
| Tester, Auditory Impedance, Exempt | PTO | 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 |
|---|---|---|---|---|---|---|
| January 3, 2025 | K242726 | Synapsys VHIT | GWN | Substantially Equivalent | Inventis S.R.L. | accessdata.fda.gov |
| March 23, 2017 | K163558 | Synapsys Ulmer Video Nystagmograph | GWN | Substantially Equivalent | Synapsys SA | accessdata.fda.gov |
Compare with other makers
- All makers of Audiometer
- All makers of Medical Device Data System
- All makers of Camera, Television, Endoscopic, With Audio
- All makers of Calibrator, Hearing Aid / Earphone And Analysis Systems
- All makers of Laryngostroboscope
- All makers of Tester, Auditory Impedance, Exempt
Updated January 3, 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.