510(k) · Cleared
ClearedAimago Easyldi Microcirculation Camera (Stand Plus Camera Arm), Aimago Easy Ldi Stand, Including 4-Wheeled Stand Base an
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Aimago SA · DPT Probe, Blood-Flow, Extravascular
Cleared on Feb 7, 2013 as substantially equivalent to K121429 (Aimago SA, 2012) after a 115-day review. Its family tree reaches back 5 generations to 1991. 1 later device descends from it.
- Decided
- Feb 7, 2013
- Review
- 115 days
- Class
- Class II
- Product code
- DPT
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 5 generations to K905232 (1991). 6 ancestors in all. 1 later device descends from it, 1 citing it directly.
- Root · 5 generations backK905232 Moor Laser Blood Flow Monitor MBF3Moor Instruments, Ltd. · 1991
- 4 generations backK980383 Mooorldi Laser Doppler ImagerMoor Instruments, Ltd. · 1998
- 3 generations backK032841 Moorldi Infrared Laser Doppler Imager, Model MOORLD12-IRMoor Instruments, Ltd. · 2003
- 2 generations backK063561 Moorldls Laser Doppler Line ScannerMoor Instruments, Ltd. · 2007
- 1 generation backK121429 Aimago Easyldi Microcirculation CameraAimago SA · 2012
- This deviceK123216 Aimago Easyldi Microcirculation Camera (Stand Plus Camera Arm)…Aimago SA · 2013
- Descendant · cites it directly · 0 of its ownK163339 Spectralmd Deepview Wound Imaging System 2.0Spectralmd, Inc. · 2017
Most influential descendants
Showing 1 of 1 · See all- K163339Spectralmd Deepview Wound Imaging System 2.0Spectralmd, Inc. · 2017 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K905232 | Moor Laser Blood Flow Monitor MBF3 | Moor Instruments, Ltd. | 1991 | — |
| −4 | K980383 | Mooorldi Laser Doppler Imager | Moor Instruments, Ltd. | 1998 | — |
| −3 | K032841 | Moorldi Infrared Laser Doppler Imager, Model MOORLD12-IR | Moor Instruments, Ltd. | 2003 | — |
| −2 | K063561 | Moorldls Laser Doppler Line Scanner | Moor Instruments, Ltd. | 2007 | — |
| −1 | K121429 | Aimago Easyldi Microcirculation Camera | Aimago SA | 2012 | — |
| 0 (this device) | K123216 | Aimago Easyldi Microcirculation Camera (Stand Plus Camera Arm), Aimago Easy… | Aimago SA | 2013 | — |
| +1 | K163339 | Spectralmd Deepview Wound Imaging System 2.0 | Spectralmd, Inc. | 2017 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1992 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2017 | 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 DPT? 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 DPT device
- #1 K233076 Laser Speckle Imaging System (RFLSI CZW)score 8.6 · 5 generations · no Class I recall
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 |
|---|---|---|---|
| * | K121429 | Aimago Easyldi Microcirculation CameraSummary page 1…are Product code: LNX Review panel: Cardiovascular Predicate Device: Substantial Equivalence is claimed with the predicate device: K121429 Aimago EasyLDl (cleared 10 August 2012) manufactured by Aimago S.A., Parc Scientifiqlue EPFL, 1015 Lausanne (Switzerland)… | 2012 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K163339 | Spectralmd Deepview Wound Imaging System 2.0 | 2017 | 0 |
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 22 years and passes through 2 companies; a new generation was cleared every 5.6 years on median.
- None of the 6 ancestors has a recall.
- Of its descendants, K163339 (Spectralmd, Inc., 2017) has gone furthest, with 0 descendants of its own.
How does its category compare?
All DPT devicesDPT Probe, Blood-Flow, Extravascular: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.
FDA decisions per year · DPT
1in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · DPT
201in 2014
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · DPT
22in 2024
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · DPT
52in 2025
MAUDE reports naming product code DPT, 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 | 3 | 55 | 0 | 5 |
| 2008 | 0 | — | 0 | 1 |
| 2009 | 1 | — | 0 | 3 |
| 2010 | 0 | — | 0 | 3 |
| 2011 | 0 | — | 0 | 3 |
| 2012 | 2 | — | 0 | 1 |
| 2013 | 3 | 108 | 0 | 0 |
| 2014 | 3 | 201 | 0 | 5 |
| 2015 | 1 | — | 0 | 0 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 1 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 3 |
| 2019 | 0 | — | 0 | 1 |
| 2020 | 0 | — | 0 | 3 |
| 2021 | 0 | — | 0 | 13 |
| 2022 | 0 | — | 0 | 46 |
| 2023 | 0 | — | 0 | 21 |
| 2024 | 1 | — | 22 | 169 |
| 2025 | 0 | — | 0 | 52 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The AMnago EasyLDI Microcirculation Camera is intended for blood flow measurements in the
microcirculation. In particular, it can be used for measuring perfusion of healthy and injured skin
including burn wounds, skin flaps (plastic and reconstructive surgery) and hand surgery.
EasyLDI Studio is intended to be used as offline viewer application for snapshots, videos and
references recorded with the Aimago EasyLDI Microcirculation Camera.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K123216 · printed Nov 6, 2026
Cite this page
510(k) Report. “K123216: Aimago Easyldi Microcirculation Camera (Stand Plus Camera Arm), Aimago Easy Ldi Stand, Including 4-Wheeled Stand Base an.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K123216
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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