510(k) · Cleared
ClearedLasersonics Tissue Morcellator Set
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Heraeus Surgical, Inc. · GCJ Laparoscope, General & Plastic Surgery
Cleared on Mar 23, 1994 after a 124-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 of the 10 devices in its family, counting itself, has a Class I recall. 9 later devices descend from it.
- Decided
- Mar 23, 1994
- Review
- 124 days
- Class
- Class II
- Product code
- GCJ
- Recalls
- None
- Predicates
- 0
9 later devices descend from it, 1 citing it directly. 1 of the 10 devices in this family, counting this one, has a Class I recall.
- This deviceK935604 Lasersonics Tissue Morcellator SetHeraeus Surgical, Inc. · 1994
- Descendant · cites it directly · 8 of its ownK980079 Coherent Tissue Morcellator Kit and AccessoriesLumenis, Inc. · 1998
- Descendant · 2 generations on · 7 of its ownK050639 Lumenis Versacut Tissue Morcellator SystemLumenis, Inc. · 2005 · Recalled (Class I)
- Descendant · 3 generations on · 5 of its ownK133272 Versacut + Tissue MorcellatorLumenis, Ltd. · 2014 · Recalled
- Descendant · 4 generations on · 2 of its ownK192499 Cyber BladeSIDAM S.r.l. · 2020
- Descendant · 4 generations on · 1 of its ownK213597 MultiCut SoloAsclepion Laser Technologies GmbH · 2023
Showing 5 of 9 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
- K050639 Lumenis Versacut Tissue Morcellator System2 generations on · 2005
Most influential descendants
Showing 5 of 9 · See all- K980079Coherent Tissue Morcellator Kit and AccessoriesLumenis, Inc. · 1998 · cites it directly8descendants
- K050639Lumenis Versacut Tissue Morcellator SystemLumenis, Inc. · 2005 · 2 generations on7descendants
- K133272Versacut + Tissue MorcellatorLumenis, Ltd. · 2014 · 3 generations on5descendants
- K192499Cyber BladeSIDAM S.r.l. · 2020 · 4 generations on2descendants
- K213597MultiCut SoloAsclepion Laser Technologies GmbH · 2023 · 4 generations on1descendant
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K935604 | Lasersonics Tissue Morcellator Set | Heraeus Surgical, Inc. | 1994 | — |
| +1 | K980079 | Coherent Tissue Morcellator Kit and Accessories | Lumenis, Inc. | 1998 | — |
| +2 | K050639 | Lumenis Versacut Tissue Morcellator System | Lumenis, Inc. | 2005 | Class I |
| +3 | K133272 | Versacut + Tissue Morcellator | Lumenis, Ltd. | 2014 | 1 |
| +4 | K192499 | Cyber Blade | SIDAM S.r.l. | 2020 | — |
| +4 | K213597 | MultiCut Solo | Asclepion Laser Technologies GmbH | 2023 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1998 | 1 | 0 |
| 2005 | 1 | 1 |
| 2011 | 1 | 0 |
| 2014 | 1 | 0 |
| 2020 | 1 | 0 |
| 2023 | 1 | 0 |
| 2024 | 1 | 0 |
| 2026 | 2 | 0 |
Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
1 device in this family has a Class I recall. 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 GCJ device
- #1 K214046 780 nm 1688 4K Camera System, 780 nm L11 LED…score 21.4 · 21 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it? (9)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K980079 | Coherent Tissue Morcellator Kit and Accessories | 1998 | 8 |
Has anything in its family been recalled? (1 Class I)
No FDA recall names this device.
Relatives with a Class I recall
Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.
- K050639Lumenis Versacut Tissue Morcellator SystemLumenis, Inc. · 2005 · 2 generations on · ◆ in the 2005 descendants bar of FIG. 11 Class I recall
What does this lineage say?
- Of its descendants, K980079 (Lumenis, Inc., 1998) has gone furthest, with 8 descendants of its own.
How does its category compare?
All GCJ devicesGCJ Laparoscope, General & Plastic Surgery: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · GCJ
21in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · GCJ
108in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GCJ
5in 2025
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · GCJ
5,860in 2025
MAUDE reports naming product code GCJ, 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 | 18 | 42 | 12 | 1,639 |
| 2008 | 19 | 73 | 16 | 1,319 |
| 2009 | 21 | 85 | 6 | 1,995 |
| 2010 | 24 | 122 | 30 | 2,657 |
| 2011 | 15 | 113 | 9 | 2,133 |
| 2012 | 17 | 88 | 1 | 1,526 |
| 2013 | 15 | 93 | 7 (1) | 1,565 |
| 2014 | 19 | 90 | 2 | 1,714 |
| 2015 | 26 | 76 | 0 | 1,710 |
| 2016 | 27 | 99 | 5 | 2,080 |
| 2017 | 20 | 77 | 1 | 3,468 |
| 2018 | 21 | 88 | 1 | 2,562 |
| 2019 | 15 | 60 | 0 | 2,578 |
| 2020 | 28 | 61 | 0 | 2,618 |
| 2021 | 18 | 116 | 0 | 3,431 |
| 2022 | 20 | 103 | 1 | 3,945 |
| 2023 | 31 | 109 | 1 | 6,002 |
| 2024 | 29 | 90 | 0 | 6,047 |
| 2025 | 21 | 108 | 5 | 5,860 |
| 2026 | 26 | 122 | 1 | — |
https://510kreport.com/device/K935604 · printed Nov 4, 2026
Cite this page
510(k) Report. “K935604: Lasersonics Tissue Morcellator Set.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K935604
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Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026