ZINNOVI INC.

FDA Device Registration & Listing · Schaumburg, IL, US · Registration 3031823608

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
3031823608
FEI Number
3031823608
Entity Name
ZINNOVI INC.
City/State/Country
Schaumburg, IL, US
Establishment Address
135 W Central Rd., Suite 204, Schaumburg, IL 60195, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Zinnovi Inc. (Owner Number: 10091122)
Owner / Operator Contact Address
135 W Central Rd., Suite 204, Schaumburg, IL 60195, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K241649
PMA Number
N/A

All Registered Proprietary Names

DUO1, DUO2

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MUH System, X-Ray, Extraoral Source, Digital Dental Class 2 872.1800 2024-07-08

Official Correspondent

Swaroop Patel

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K221008 Shanghai Handy Medical Equipment Co., Ltd. HDR Sensor- HDR361 (Size 1), HDR Sensor- HDR461 (Size 2) 2022-06-22
K160788 Ray Co., Ltd. RIOScan (RPS500) 2016-04-15

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3031823608. Last updated year: 2026. Please use registration number 3031823608 when referencing this establishment in official correspondence.
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