Data / Medical devices / United States / TendoNova Corporation
TendoNova Corporation: FDA-registered device maker in Atlanta, GA, United States, 1 510(k) clearance
TendoNova Corporation is registered with the FDA (registration 3025663926) in Atlanta, GA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 8, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3025663926
- Address
- 75 5th St Nw Ste 2160, Atlanta, GA, United States, 30308
- Owner or operator
- TendoNova Corporation (10086875)
- Roles
- Manufacturer
- First device listed
- December 19, 2022
- Registered through
- 2026
- Brand names listed
- Ocelot Nano TDS 1000
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Instrument, Ultrasonic Surgical | LFL | U | 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 |
|---|---|---|---|---|---|---|
| March 8, 2022 | K212049 | Oclet TDS 1000 | LFL | Substantially Equivalent | Tendonova Corporation | accessdata.fda.gov |
Compare with other makers
Updated March 8, 2022. 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.