ACTIVBODY

FDA Device Registration & Listing · San Diego, CA, US · Registration 3015316271

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
3015316271
FEI Number
3015316271
Entity Name
ACTIVBODY
City/State/Country
San Diego, CA, US
Establishment Address
4350 Executive Drive, Suite 200, San Diego, CA 92121, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
ActivBody (Owner Number: 10085316)
Owner / Operator Contact Address
4350 Executive Drive, Suite 200, San Diego, CA 92121, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Activforce 2

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KQX Goniometer, Ac-Powered Orthopedic Class 1 888.1500 2025-09-04

Official Correspondent

Tay Nguyen

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ActivBody
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 3015316271. Last updated year: 2026. Please use registration number 3015316271 when referencing this establishment in official correspondence.
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