510(k) · Cleared
ClearedSKIA-Head (Model: SKIA-ST00)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Skia, Inc. · LLZ System, Image Processing, Radiological
Cleared on Feb 23, 2026 as substantially equivalent to K223125 (Mediview Xr, Inc., 2023) and 1 other predicate after a 129-day review. Its family tree reaches back 14 generations to 1991.
- Decided
- Feb 23, 2026
- Review
- 129 days
- Class
- Class II
- Product code
- LLZ
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 14 generations to K913770 (1991). 58 ancestors in all, the oldest K896095 (1990). No later device cites it as a predicate yet.
- Root · 14 generations backK913770 Advantage V.S. CT/MR Rad Diagnostic WorkstationGeneral Electric Co. · 1991
- 10 generations between
- 3 generations backK163232 Vitrea ViewVital Images, Inc. · 2017
- 2 generations backK190764 SurgicalARMedivis, Inc. · 2019
- 1 generation backK230249 IkshanaImmersivetouch · 2023
- This deviceK253486 SKIA-Head (Model: SKIA-ST00)Skia, Inc. · 2026
Show all 14 generations
- Root · 14 generations backK913770 Advantage V.S. CT/MR Rad Diagnostic WorkstationGeneral Electric Co. · 1991
- 13 generations backK960613 GE Advantage Windows Review WorkstationGE Medical Systems · 1996
- 12 generations backK020483 Advantage Workstation 4.1GE Medical Systems · 2002 · Recalled
- 11 generations backK023003 Imagechecker-CT WorkstationR2 Technology, Inc. · 2002
- 10 generations backK032748 VITREA2, Version 3.4 Medical Image Processing SoftwareVital Images, Inc. · 2003 · Recalled
- 9 generations backK040305 VITREA2 Version 3.5Vital Images, Inc. · 2004
- 8 generations backK043333 VITREA2, Version 3.7 Medical Image Processing SystemVital Images, Inc. · 2004 · Recalled
- 7 generations backK052632 VITREA2 Version 3.8 Medical Image Processing SoftwareVital Images, Inc. · 2005 · Recalled
- 6 generations backK061624 Vitrea, Version 3.9Vital Images, Inc. · 2006 · Recalled
- 5 generations backK071362 Vital Connect 4.1Vital Images, Inc. · 2007 · Recalled
- 4 generations backK150738 VitreaViewVital Images, Inc. · 2015
- 3 generations backK163232 Vitrea ViewVital Images, Inc. · 2017
- 2 generations backK190764 SurgicalARMedivis, Inc. · 2019
- 1 generation backK230249 IkshanaImmersivetouch · 2023
- This deviceK253486 SKIA-Head (Model: SKIA-ST00)Skia, Inc. · 2026
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −14 | K913770 | Advantage V.S. CT/MR Rad Diagnostic Workstation | General Electric Co. | 1991 | — |
| −13 | K960613 | GE Advantage Windows Review Workstation | GE Medical Systems | 1996 | — |
| −12 | K020483 | Advantage Workstation 4.1 | GE Medical Systems | 2002 | 2 |
| −11 | K023003 | Imagechecker-CT Workstation | R2 Technology, Inc. | 2002 | — |
| −10 | K032748 | VITREA2, Version 3.4 Medical Image Processing Software | Vital Images, Inc. | 2003 | 2 |
| −9 | K040305 | VITREA2 Version 3.5 | Vital Images, Inc. | 2004 | — |
| −8 | K043333 | VITREA2, Version 3.7 Medical Image Processing System | Vital Images, Inc. | 2004 | 1 |
| −7 | K052632 | VITREA2 Version 3.8 Medical Image Processing Software | Vital Images, Inc. | 2005 | 2 |
| −6 | K061624 | Vitrea, Version 3.9 | Vital Images, Inc. | 2006 | 1 |
| −5 | K071362 | Vital Connect 4.1 | Vital Images, Inc. | 2007 | 3 |
| −4 | K150738 | VitreaView | Vital Images, Inc. | 2015 | — |
| −3 | K163232 | Vitrea View | Vital Images, Inc. | 2017 | — |
| −2 | K190764 | SurgicalAR | Medivis, Inc. | 2019 | — |
| −1 | K230249 | Ikshana | Immersivetouch | 2023 | — |
| 0 (this device) | K253486 | SKIA-Head (Model: SKIA-ST00) | Skia, Inc. | 2026 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1990 | 1 | 0 |
| 1991 | 2 | 0 |
| 1994 | 3 | 0 |
| 1995 | 1 | 0 |
| 1996 | 4 | 0 |
| 1997 | 2 | 0 |
| 1998 | 4 | 0 |
| 1999 | 2 | 0 |
| 2000 | 3 | 0 |
| 2001 | 7 | 0 |
| 2002 | 3 | 0 |
| 2004 | 4 | 0 |
| 2005 | 1 | 0 |
| 2006 | 1 | 0 |
| 2010 | 1 | 0 |
| 2011 | 1 | 0 |
| 2012 | 1 | 0 |
| 2019 | 1 | 0 |
| 2021 | 1 | 0 |
| 2023 | 1 | 0 |
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 LLZ? 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 LLZ device
- #1 K230955 syngo Application Softwarescore 21.5 · 11 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
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 |
|---|---|---|---|
| * | K223125 | XR90 (XR90-Sys)Summary page 6…cking, or stereotactic guidance. This device is intended for prescription use only (Rx Only). Primary Predicate Device XR90 (Model: XR90-SYS, MediView XR, Inc. K223125, 07/13/2023) - Common Name: System, Image Processing, Radiological - Regulation Name: Medical Image Management and… | 2023 |
| * | K230249 | IkshanaSummary page 6…Code: LLZ - Regulation Number: 21 CFR 892.2050 - Classification Panel: Radiology Secondary Predicate Device Ikshana (ImmersiveAR, ImmersiveTouch K230249, 10/16/2023) - Common Name: System, Image Processing, Radiological - Regulation Name: Medical Image Management and… | 2023 |
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 35 years and passes through 7 companies; a new generation was cleared every 1.8 years on median.
- 14 of the 58 ancestors have a recall of any class.
How does its category compare?
All LLZ devicesLLZ System, Image Processing, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.
FDA decisions per year · LLZ
58in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LLZ
173in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LLZ
11in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · LLZ
116in 2025
MAUDE reports naming product code LLZ, 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 | 76 | 36 | 20 | 152 |
| 2008 | 94 | 52 | 32 | 154 |
| 2009 | 70 | 62 | 21 | 145 |
| 2010 | 51 | 98 | 17 | 145 |
| 2011 | 106 | 79 | 30 | 454 |
| 2012 | 82 | 87 | 12 | 266 |
| 2013 | 95 | 84 | 64 | 1,130 |
| 2014 | 78 | 89 | 6 | 15,631 |
| 2015 | 64 | 90 | 16 | 211 |
| 2016 | 82 | 90 | 12 | 290 |
| 2017 | 78 | 107 | 5 | 104 |
| 2018 | 104 | 105 | 7 | 72 |
| 2019 | 74 | 107 | 2 | 88 |
| 2020 | 81 | 115 | 6 | 82 |
| 2021 | 83 | 116 | 3 | 70 |
| 2022 | 65 | 137 | 4 | 28 |
| 2023 | 87 | 157 | 8 | 26 |
| 2024 | 62 | 131 | 6 | 42 |
| 2025 | 58 | 173 | 11 | 116 |
| 2026 | 45 | 110 | 14 | — |
What is it indicated for?
The SKIA-Head (SKIA-ST00) is a medical display system intended for 3D image visualization and image interaction in conjunction with traditional imaging and monitors. The virtual images are generated from 3D volumetric data previously acquired from CT sources and visualized to 3D patient images being displayed on a tablet PC using 3D cameras. The device is intended to provide visual information and reference to be used by health care professionals for…
Read the full statement (187 words)
The SKIA-Head (SKIA-ST00) is a medical display system intended for 3D image visualization and image interaction in conjunction with traditional imaging and monitors. The virtual images are generated from 3D volumetric data previously acquired from CT sources and visualized to 3D patient images being displayed on a tablet PC using 3D cameras.
The device is intended to provide visual information and reference to be used by health care professionals for analysis of surgical options during pre-operative planning.
The device may also be used in a limited, early intraoperative context, specifically during phases in which the patient’s skin surface remains consistent with the CT-acquired skin surface model. This generally corresponds to the period after anesthesia but before any manipulation that would deform or alter the patient’s external skin surface. This represents a pre-operative to early intraoperative transition phase, during which the patient’s posture is fixed and the skin surface remains sufficiently stable for skin-based registration.
The system is intended for visualization and reference purposes only and is not intended for real-time surgical navigation, instrument tracking, or stereotactic guidance.
This device is intended for prescription use only (Rx Only).
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K253486 · printed Nov 4, 2026
Cite this page
510(k) Report. “K253486: SKIA-Head (Model: SKIA-ST00).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K253486
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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