TendoNova Corporation

FDA Device Registration & Listing · Atlanta, GA, US · Registration 3025663926

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3025663926
FEI Number
3025663926
Entity Name
TendoNova Corporation
City/State/Country
Atlanta, GA, US
Establishment Address
75 5th St Nw Ste 2160, Atlanta, GA 30308, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
TendoNova Corporation (Owner Number: 10086875)
Owner / Operator Contact Address
75 Fifth Street NW, Suite 2160, Atlanta, GA 30308, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K212049
PMA Number
N/A

All Registered Proprietary Names

Ocelot Nano TDS 1000

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LFL Instrument, Ultrasonic Surgical Unknown Class U N/A 2022-12-19

Official Correspondent

Brett Rodgers

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TendoNova Corporation
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0332-2022 Covidien Llc U
Covidien Sonicision Battery Charger-intended to charge the Sonicision Reusable Battery Pack and to provide information on the battery charging progress and battery pack status Item Code: CBCA

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3025663926. Last updated year: 2026. Please use registration number 3025663926 when referencing this establishment in official correspondence.
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