510(k) · Cleared
ClearedRadioLens v1.0
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Synapsica · QIH Automated Radiological Image Processing Software
Cleared on Mar 28, 2023 as substantially equivalent to K221632 (Medical Metrics, Inc., 2022) after a 250-day review. Its family tree reaches back 2 generations to 2002.
- Decided
- Mar 28, 2023
- Review
- 250 days
- Class
- Class II
- Product code
- QIH
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K022585 (2002). No later device cites it as a predicate yet.
View FIG. 1 as a table
Line of descent and top descendants
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in QIH? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new QIH device
- #1 K213998 cvi42 Auto Imaging Software Applicationscore 23.5 · 7 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K221632 | Spine CAMP™ Cleared while this submission was under review Summary page 4…de QIH Regulatory Class II 3. Predicate Device Proprietary Name Spine CAMP™ Premarket Notification K221632 Classification Name Automated Radiological Image Processing Software Regulation Number 21 CFR 892.2… | 2022 |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 21 years and passes through 2 companies; a new generation was cleared every 20.0 years on median.
- None of the 2 ancestors has a recall.
- 1 other device also cites its predicate K221632.
How does its category compare?
All QIH devicesQIH Automated Radiological Image Processing Software: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.
FDA decisions per year · QIH
94in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · QIH
150in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · QIH
1so far in 2026, the most since 2007
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · QIH
4in 2025
MAUDE reports naming product code QIH, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 2 | — | 0 | 0 |
| 2020 | 11 | 145 | 0 | 0 |
| 2021 | 19 | 125 | 0 | 0 |
| 2022 | 25 | 134 | 0 | 0 |
| 2023 | 45 | 151 | 0 | 0 |
| 2024 | 64 | 141 | 0 | 2 |
| 2025 | 94 | 150 | 0 | 4 |
| 2026 | 78 | 130 | 1 | — |
What is it indicated for?
RadioLens v1.0 software is a medical diagnostic application that displays, processes, stores, and transfers DICOM data, with the exception of mammography. It provides the capability to store images and patient information, perform filtering, digital manipulation, and quantitative measurements. The client software is designed to run on standard personal and business computers. RadioLens v1.0 includes an optional SpindleX module which is used to analyze…
Read the full statement (176 words)
RadioLens v1.0 software is a medical diagnostic application that displays, processes, stores, and transfers DICOM data, with the exception of mammography. It provides the capability to store images and patient information, perform filtering, digital manipulation, and quantitative measurements. The client software is designed to run on standard personal and business computers.
RadioLens v1.0 includes an optional SpindleX module which is used to analyze potential vertebral body displacements in spine, either absolute or relative, using cervical/lumbar digital X-Rays of spine. A qualified medical practitioner may use the module to semi-automatically identify relevant spine anatomy and calculate vertebral displacement measurements. Measurements are then used to determine severity and location of any spinal ligament injury leading to subluxation using criteria published in AMA Guides to The Evaluation of Permanent Impairment, 5th & 6th edition.
SpindleX is meant for assistance with analysis of spinal ligament injury in the adult population (>18 years of age) as captured in stress x-rays. SpindleX is not meant for patients that have undergone surgery or other traumatic injury that result in distortion of spinal anatomy.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K222174 · printed Nov 6, 2026
Cite this page
510(k) Report. “K222174: RadioLens v1.0.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K222174
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026