510(k) · Cleared
ClearedCyberwand Lithotripter
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Cybersonics, Inc. · FFK Lithotriptor, Electro-Hydraulic
Cleared on Aug 30, 2010 as substantially equivalent to K052135 (Cybersonics, Inc., 2005) after a 28-day review. Its family tree reaches back 4 generations to 1986. 5 later devices descend from it.
- Decided
- Aug 30, 2010
- Review
- 28 days
- Class
- Class II
- Product code
- FFK
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 4 generations to K863642 (1986). 8 ancestors in all. 5 later devices descend from it, 2 citing it directly.
- Root · 4 generations backK863642 Candela Model MDL-1 Laser LithotriptorCandela Corp. · 1986
- 3 generations backK963285 Ems Swiss Lithoclast LithotripterElectro Medical Systems SA · 1997
- 2 generations backK012445 Ems Swiss Lithoclast Master (a.K.a. Swiss Lithoclast Ultra)Electro Medical Systems SA · 2001 · Recalled
- 1 generation backK052135 Cybersonics Cyberwand Dual Probe LithotripterCybersonics, Inc. · 2005 · Recalled
- This deviceK102169 Cyberwand LithotripterCybersonics, Inc. · 2010
- Descendant · cites it directly · 3 of its ownK120303 Cyberwand Dual Action Ultrasonic Lithotripsy SystemCybersonics, Inc. · 2012
- Descendant · 2 generations on · 1 of its ownK142428 Shock Pulse-SE Lithotripsy System CYBERWAND IICybersonics, Inc. · 2014 · Recalled
- Descendant · 3 generations on · 0 of its ownK171024 ShockPulse-SE Lithotripsy SystemCybersonics, Inc. · 2017 · Recalled
- Descendant · 2 generations on · 0 of its ownK132795 Cyberwand Sterile Probe SetCybersonics, Inc. · 2013
- Descendant · cites it directly · 0 of its ownK111058 Uretron Model UrtMed-Sonics Corp. · 2012
Most influential descendants
Showing 5 of 5 · See all- K120303Cyberwand Dual Action Ultrasonic Lithotripsy SystemCybersonics, Inc. · 2012 · cites it directly3descendants
- K142428Shock Pulse-SE Lithotripsy System CYBERWAND IICybersonics, Inc. · 2014 · 2 generations on1descendant
- K171024ShockPulse-SE Lithotripsy SystemCybersonics, Inc. · 2017 · 3 generations on0descendants
- K132795Cyberwand Sterile Probe SetCybersonics, Inc. · 2013 · 2 generations on0descendants
- K111058Uretron Model UrtMed-Sonics Corp. · 2012 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K863642 | Candela Model MDL-1 Laser Lithotriptor | Candela Corp. | 1986 | — |
| −3 | K963285 | Ems Swiss Lithoclast Lithotripter | Electro Medical Systems SA | 1997 | — |
| −2 | K012445 | Ems Swiss Lithoclast Master (a.K.a. Swiss Lithoclast Ultra) | Electro Medical Systems SA | 2001 | 3 |
| −1 | K052135 | Cybersonics Cyberwand Dual Probe Lithotripter | Cybersonics, Inc. | 2005 | 1 |
| 0 (this device) | K102169 | Cyberwand Lithotripter | Cybersonics, Inc. | 2010 | — |
| +1 | K120303 | Cyberwand Dual Action Ultrasonic Lithotripsy System | Cybersonics, Inc. | 2012 | — |
| +2 | K142428 | Shock Pulse-SE Lithotripsy System CYBERWAND II | Cybersonics, Inc. | 2014 | 1 |
| +3 | K171024 | ShockPulse-SE Lithotripsy System | Cybersonics, Inc. | 2017 | 6 |
| +2 | K132795 | Cyberwand Sterile Probe Set | Cybersonics, Inc. | 2013 | — |
| +1 | K111058 | Uretron Model Urt | Med-Sonics Corp. | 2012 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1989 | 1 | 0 |
| 1992 | 1 | 0 |
| 1995 | 1 | 0 |
| 1998 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2012 | 2 | 0 |
| 2013 | 1 | 0 |
| 2014 | 1 | 0 |
| 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 FFK? 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 FFK device
- #1 K230488 EL27-Compact; Sterile EHL-Probesscore 12.2 · 2 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 |
|---|---|---|---|
| * | K052135 | Cybersonics Cyberwand Dual Probe LithotripterSummary page 1…hotripter Predicate Device(s): The CyberWand Hollow Semi-Flexible Ureteral probe is equivalent to the Cyberwand Dual Probe Set (1K052135). Device Description: The CyberWand Dual Ultrasonic Lithotripsy System is an electrom… | 2005 |
What descends from it? (5)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
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 24 years and passes through 3 companies; a new generation was cleared every 4.7 years on median.
- 2 of the 8 ancestors have a recall of any class.
- Of its descendants, K120303 (Cybersonics, Inc., 2012) has gone furthest, with 3 descendants of its own.
- 2 other devices also cite its predicate K052135.
How does its category compare?
All FFK devicesFFK Lithotriptor, Electro-Hydraulic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.
FDA decisions per year · FFK
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FFK
110in 2013
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FFK
1in 2021
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · FFK
6in 2025
MAUDE reports naming product code FFK, 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 | 2 | — | 1 | 6 |
| 2008 | 0 | — | 0 | 12 |
| 2009 | 0 | — | 1 | 35 |
| 2010 | 2 | — | 0 | 16 |
| 2011 | 0 | — | 0 | 6 |
| 2012 | 2 | — | 0 | 2 |
| 2013 | 3 | 110 | 0 | 10 |
| 2014 | 0 | — | 0 | 9 |
| 2015 | 0 | — | 0 | 7 |
| 2016 | 2 | — | 0 | 7 |
| 2017 | 0 | — | 1 | 9 |
| 2018 | 0 | — | 0 | 18 |
| 2019 | 1 | — | 0 | 10 |
| 2020 | 0 | — | 0 | 39 |
| 2021 | 1 | — | 1 | 22 |
| 2022 | 0 | — | 0 | 13 |
| 2023 | 1 | — | 0 | 10 |
| 2024 | 0 | — | 0 | 8 |
| 2025 | 2 | — | 0 | 6 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The CyberWand Hollow Semi-Flexible Ureteral probe is designed to be used only with the CyberWand System for the fragmentation of urinary tract calculi in the kidneys, ureter, and bladder.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K102169 · printed Nov 6, 2026
Cite this page
510(k) Report. “K102169: Cyberwand Lithotripter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K102169
Report an extraction error
Are you the manufacturer?
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