ANODYNE

FDA Device Registration & Listing · Milwaukee, WI, US · Registration 3011654627

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
3011654627
FEI Number
3011654627
Entity Name
ANODYNE
City/State/Country
Milwaukee, WI, US
Establishment Address
5050 S 2nd St, Milwaukee, WI 53207, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Anodyne (Owner Number: 10049577)
Owner / Operator Contact Address
5050 S 2nd St, Milwaukee, WI 53207, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Anodyne Anodyne

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FQL Stocking, Medical Support (For General Medical Purposes) General Hospital Class 1 880.5780 2022-08-05
KNP Orthosis, Corrective Shoe Physical Medicine Class 1 890.3475 2015-06-22
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 2015-06-22

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011654627. Last updated year: 2026. Please use registration number 3011654627 when referencing this establishment in official correspondence.
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