CADENSE INC

FDA Device Registration & Listing · Goleta, CA, US · Registration 3039167356

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
3039167356
FEI Number
3039167356
Entity Name
CADENSE INC
City/State/Country
Goleta, CA, US
Establishment Address
Cremona Drive, Suite 210, Goleta, CA 93117, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Cadense Inc (Owner Number: 10093690)
Owner / Operator Contact Address
935 West Campus Lane, Goleta, CA 93117, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Cadense Cadense Original Havena AERIO

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNP Orthosis, Corrective Shoe Physical Medicine Class 1 890.3475 2025-06-24

Official Correspondent

Johannes Sauer

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cadense Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3039167356. Last updated year: 2026. Please use registration number 3039167356 when referencing this establishment in official correspondence.
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