APIXIA INC.

FDA Device Registration & Listing · City of Industry, CA, US · Registration 3008361230

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
3008361230
FEI Number
3008361230
Entity Name
APIXIA INC.
City/State/Country
City of Industry, CA, US
Establishment Address
18688 E. SAN JOSE AVE, City of Industry, CA 91748, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
APIXIA INC. (Owner Number: 10031841)
Owner / Operator Contact Address
18688 E. SAN JOSE AVE, City of Industry, CA 91748, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KQM Camera, Surgical And Accessories General, Plastic Surgery Class 1 878.4160 2010-10-06
IWZ Film, Radiographic Radiology Class 1 892.1840 2010-08-13
EHA Aligner, Beam, X-Ray Dental Class 1 872.1820 2010-08-13
MUH System, X-Ray, Extraoral Source, Digital Dental Class 2 872.1800 2012-05-11
EHD Unit, X-Ray, Extraoral With Timer Dental Class 2 872.1800 2010-06-11
NRD Unit, Operative Dental, Accessories Dental Class 1 872.6640 2011-03-01
EGZ Holder, Film, X-Ray Dental Class 1 872.1905 2010-08-13

Official Correspondent

JERRY HUANG

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

APIXIA 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
K991310 Villa Sistemi Medicali S.P.A. EXPLOR-X 70 1999-06-18

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0009-2015 Gendex Corp 2
eXpertDC intraoral x-ray, models: eXpert DC, NA, 75 Inch reach; eXpert DC, NA, 65 Inch reach; eXpert DC, CN, 55 Inch reach; eXpert DC, WW, 75 Inch reach; eXpert DC, WW, 65 Inch reach; eXpert DC, WW, 55 Inch reach; OEM Arm Assembly w/o cables; Assy, Articulated Arm & Tubehead, eDC; and Assy, Articulated Arm & Tubehead, 765DC Product Usage: intraoral x-ray
Z-0016-2017 Panoramic Rental Corp. 2
Panoramic X-ray Model PC-1000, Laser-1000 packed in a crate Product Usage: The PC-1000 will enable the user to take panoramic x-ray images. The PC-1000/Laser1000 will enable the user to take panoramic x-ray images as well as cephalometric x-ray images.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008361230. Last updated year: 2026. Please use registration number 3008361230 when referencing this establishment in official correspondence.
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