510(k) · Decided
DecidedLeica FL560
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Leica Microsystems (Schweiz) AG · IZI System, X-Ray, Angiographic
Cleared on Jul 5, 2017 as substantially equivalent to K141136 (Leica Biosystems Richmond, 2014) and 2 other predicates after a 160-day review. Its family tree reaches back 7 generations to 1994.
- Decided
- Jul 5, 2017
- Review
- 160 days
- Class
- Class II
- Product code
- IZI
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 7 generations to K944261 (1994). 10 ancestors in all. No later device cites it as a predicate yet.
- Root · 7 generations backK944261 Retina AngiographHeidelberg Engineering · 1994
- 6 generations backK042961 Spy Intra-Operative Imaging System: SP2000Novadaq Technologies, Inc. · 2005 · Recalled
- 5 generations backK060867 Spy Intraoperative Imaging SystemNovadaq Technologies, Inc. · 2006 · Recalled
- 4 generations backK063345 Spy Imaging SystemNovadaq Technologies, Inc. · 2007 · Recalled
- 3 generations backK072222 Spy Fluorescent Imaging SystemNovadaq Technologies, Inc. · 2007 · Recalled
- 2 generations backK080612 Leica FL800Leica Microsystems (Schweiz) AG · 2008
- 1 generation backK141136 Leica FL800Leica Biosystems Richmond · 2014
- This deviceK170239 Leica FL560Leica Microsystems (Schweiz) AG · 2017
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −7 | K944261 | Retina Angiograph | Heidelberg Engineering | 1994 | — |
| −6 | K042961 | Spy Intra-Operative Imaging System: SP2000 | Novadaq Technologies, Inc. | 2005 | 1 |
| −5 | K060867 | Spy Intraoperative Imaging System | Novadaq Technologies, Inc. | 2006 | 1 |
| −4 | K063345 | Spy Imaging System | Novadaq Technologies, Inc. | 2007 | 1 |
| −3 | K072222 | Spy Fluorescent Imaging System | Novadaq Technologies, Inc. | 2007 | 1 |
| −2 | K080612 | Leica FL800 | Leica Microsystems (Schweiz) AG | 2008 | — |
| −1 | K141136 | Leica FL800 | Leica Biosystems Richmond | 2014 | — |
| 0 (this device) | K170239 | Leica FL560 | Leica Microsystems (Schweiz) AG | 2017 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1999 | 1 | 0 |
| 2006 | 1 | 0 |
| 2007 | 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 IZI? 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 IZI device
- #1 K230727 SPY Portable Handheld Imaging (SPY-PHI) Systemscore 23.2 · 20 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (3)
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 |
|---|---|---|---|
| * | K141136 | Leica FL800Summary page 5…+353 86 7710135 email [email protected] Predicate Device Primary Leica FL800 ULT – clearance K141136 Auxiliary Leica FL800 – clearance K061871 & K080612 Preparation Date 20th December 2016… | 2014 |
| * | K061871 | Leica Model FL800Summary page 5…[email protected] Predicate Device Primary Leica FL800 ULT – clearance K141136 Auxiliary Leica FL800 – clearance K061871 & K080612 Preparation Date 20th December 2016 Device Description Similar to the predicate device (Leica FL800 ULT… | 2006 |
| * | K080612 | Leica FL800Summary page 5…@leica-microsystems.com Predicate Device Primary Leica FL800 ULT – clearance K141136 Auxiliary Leica FL800 – clearance K061871 & K080612 Preparation Date 20th December 2016 Device Description Similar to the predicate device (Leica FL800 ULT approved u… | 2008 |
| † | K092374 | Ois Eyescan Portable Modular Imaging System, Model Ois Eyescan | 2009 |
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 23 years and passes through 4 companies; a new generation was cleared every 1.3 years on median.
- 6 of the 10 ancestors have a recall of any class.
- 2 other devices also cite its predicate K141136.
How does its category compare?
All IZI devicesIZI System, X-Ray, Angiographic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.
FDA decisions per year · IZI
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · IZI
81in 2023
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · IZI
1in 2021
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · IZI
2,171in 2025
MAUDE reports naming product code IZI, 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 | 7 | 28 | 6 | 92 |
| 2008 | 6 | 68 | 52 | 101 |
| 2009 | 2 | — | 18 | 132 |
| 2010 | 2 | — | 11 | 252 |
| 2011 | 4 | 104 | 6 | 377 |
| 2012 | 1 | — | 6 | 77 |
| 2013 | 1 | — | 6 | 58 |
| 2014 | 4 | 111 | 5 | 123 |
| 2015 | 0 | — | 14 | 36 |
| 2016 | 1 | — | 7 | 102 |
| 2017 | 2 | — | 1 | 88 |
| 2018 | 2 | — | 2 | 49 |
| 2019 | 2 | — | 2 | 30 |
| 2020 | 1 | — | 2 | 14 |
| 2021 | 1 | — | 1 | 29 |
| 2022 | 1 | — | 0 | 265 |
| 2023 | 3 | 81 | 0 | 1,204 |
| 2024 | 2 | — | 0 | 1,332 |
| 2025 | 2 | — | 0 | 2,171 |
| 2026 | 2 | — | 1 | — |
What is it indicated for?
The Leica FL560 is a surgical microscope accessory used in viewing intra-operative blood flow in the cerebral vascular area.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K170239 · printed Nov 3, 2026
Cite this page
510(k) Report. “K170239: Leica FL560.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K170239
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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