CARDEA TECHNOLOGY, INC.

FDA Device Registration & Listing · Arlington, MA, US · Registration 3007867472

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
3007867472
FEI Number
3007867472
Entity Name
CARDEA TECHNOLOGY, INC.
City/State/Country
Arlington, MA, US
Establishment Address
1337 Mass Ave, #266, Arlington, MA 02476, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Cardea Technology, Inc. (Owner Number: 10023643)
Owner / Operator Contact Address
1337 Mass Ave, #266, Arlington, MA 02476, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

BoneStation

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LMD System, Digital Image Communications, Radiological Radiology Class 1 892.2020 2007-12-06

Official Correspondent

Nadine Thomas

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cardea Technology, Inc.
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 3007867472. Last updated year: 2026. Please use registration number 3007867472 when referencing this establishment in official correspondence.
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