Data / Medical devices / United States / Resonance of America, Inc
Resonance of America, Inc: FDA-registered device maker in New York, NY, United States, 1 510(k) clearance
Resonance of America, Inc is registered with the FDA (registration 3026566521) in New York, NY, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 21, 2003. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3026566521
- Address
- 48 Wall St Ste 1100, New York, NY, United States, 10005
- Owner or operator
- M.R.S. Srl (10045540)
- Roles
- Complaint file establishment
- First device listed
- November 27, 2013
- Registered through
- 2026
- Brand names listed
- R07A, R140, R15C, R15C-T, R16M, R17A, R25C, R25CPT and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Audiometer | EWO | 2 | Complaint file establishment | accessdata.fda.gov |
| Medical Device Data System | OUG | 1 | Complaint file establishment | accessdata.fda.gov |
| Otoscope | ERA | 1 | Complaint file establishment | accessdata.fda.gov |
| Tester, Auditory Impedance | ETY | 2 | Complaint file establishment | 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 |
|---|---|---|---|---|---|---|
| July 21, 2003 | K031978 | AMPLAID A756 SCREENING ADMITTANCE METER | ETY | Substantially Equivalent | Amplaid | accessdata.fda.gov |
Compare with other makers
- All makers of Audiometer
- All makers of Tester, Auditory Impedance
- All makers of Medical Device Data System
- All makers of Otoscope
Updated July 21, 2003. 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.