INKSPACE IMAGING, INC

FDA Device Registration & Listing · Pleasanton, CA, US · Registration 3021244844

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
3021244844
FEI Number
3021244844
Entity Name
INKSPACE IMAGING, INC
City/State/Country
Pleasanton, CA, US
Establishment Address
5635 West Las Positas Blvd, Suite 403/404, Pleasanton, CA 94588, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Inkspace Imaging, Inc (Owner Number: 10083875)
Owner / Operator Contact Address
5635 West Las Positas Blvd, Suite 403/404, Pleasanton, CA 94588, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K253182
PMA Number
N/A

All Registered Proprietary Names

Snuggle; Silhouette; Nuzzle InkSpace Imaging Body Array InkSpace Imaging Pediatric Body Array InkSpace Imaging Small Body Array Snuggle Pediatric Array Silhouette Adult Array Small Body Array

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MOS Coil, Magnetic Resonance, Specialty Radiology Class 2 892.1000 2025-08-07
MOS Coil, Magnetic Resonance, Specialty Radiology Class 2 892.1000 2023-10-04
MOS Coil, Magnetic Resonance, Specialty Radiology Class 2 892.1000 2021-12-27
MOS Coil, Magnetic Resonance, Specialty Radiology Class 2 892.1000 2024-01-25
MOS Coil, Magnetic Resonance, Specialty Radiology Class 2 892.1000 2026-01-08

Official Correspondent

My Nguyen

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Inkspace Imaging, 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
K121249 Paramed S.R.L. MULTIARRAY KIT 2012-06-12
K000935 Mri Devices Corp. KFA-63 KNEE AND FOOT ARRAY 2000-04-07
K102889 Hitachi Medical Systems America, Inc. HITACHI ECHELON NV ATTACHMENT AND SMALL EXTREMITY COILS MODEL ECHELON 2010-12-20
K110373 Esaote, S.p.A. TEMPOROMANIBULAR COIL 15 2011-04-06
K030317 Midwest Rf, LLC MODEL 1300GE-64: PEDIATRIC POSITIONER 2003-03-25

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-2020 Quality Electrodynamics LLC 2
TxRx 15Ch Knee Coil 3T QED part number:Q7000008 Siemens Model # 10185460
Z-0032-2020 Quality Electrodynamics LLC 2
TxRx 15CH Knee Coil 1.5T QED part number:Q7000016 Siemens Model # 10185453
Z-0033-2020 Quality Electrodynamics LLC 2
TxRx CP Extremity Coil 3T QED part number: Q7000019 Siemens Model # 10185464
Z-0034-2020 Quality Electrodynamics LLC 2
TxRx 15CH Knee Coil 1.5T QED part number: Q7000050 Siemens Model # 10606524
Z-0035-2020 Quality Electrodynamics LLC 2
TxRx 15CH Knee Coil 3T QED part number: Q7000051 Siemens Model # 10606525

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021244844. Last updated year: 2026. Please use registration number 3021244844 when referencing this establishment in official correspondence.
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