510(k) · Cleared
ClearedEnable Endoscopic Bipolar Scissors
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Enable Medical Corp. · GEI Electrosurgical, Cutting & Coagulation & Accessories
Cleared on Nov 24, 1999 as substantially equivalent to K950286 (Symbiosis Corp., 1995) and 6 other predicates after a 78-day review. Its family tree reaches back 3 generations to 1994. 7 later devices descend from it.
- Decided
- Nov 24, 1999
- Review
- 78 days
- Class
- Class II
- Product code
- GEI
- Recalls
- None
- Predicates
- 7
Its longest line of descent runs back 3 generations to K945975 (1994). 9 ancestors in all. 7 later devices descend from it, 1 citing it directly.
- Root · 3 generations backK945975 Evershears (R) Scissors, Bilap (R) Probes, Bicoag (R) ForcepsEverest Medical Corp. · 1994
- 2 generations backK972558 Bipolar ScissorsEnable Medical Corp. · 1997
- 1 generation backK981219 Oscar Bipolar Scissors and Oscar Bipolar Reusable CartridgesEnable Medical Corp. · 1998
- This deviceK992996 Enable Endoscopic Bipolar ScissorsEnable Medical Corp. · 1999
- Descendant · cites it directly · 6 of its ownK001330 Sovereign Bipolar InstrumentsAesculap, Inc. · 2000
- Descendant · 2 generations on · 3 of its ownK030890 SwitchbladeSnowden Pencer, Inc. · 2003
- Descendant · 3 generations on · 1 of its ownK113407 Snowden Pencer Laparoscopic Ergonomic Reposable ScissorsCarefusion 2200, Inc. · 2012
- Descendant · 2 generations on · 0 of its ownK160393 AdTecAesculap, Inc. · 2016
- Descendant · 4 generations on · 0 of its ownK132232 Mins Needlescopic Resposable Device SystemMinilap Technologies · 2013
Showing 5 of 7 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 7 · See all- K001330Sovereign Bipolar InstrumentsAesculap, Inc. · 2000 · cites it directly6descendants
- K030890SwitchbladeSnowden Pencer, Inc. · 2003 · 2 generations on3descendants
- K113407Snowden Pencer Laparoscopic Ergonomic Reposable ScissorsCarefusion 2200, Inc. · 2012 · 3 generations on1descendant
- K160393AdTecAesculap, Inc. · 2016 · 2 generations on0descendants
- K132232Mins Needlescopic Resposable Device SystemMinilap Technologies · 2013 · 4 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K945975 | Evershears (R) Scissors, Bilap (R) Probes, Bicoag (R) Forceps | Everest Medical Corp. | 1994 | — |
| −2 | K972558 | Bipolar Scissors | Enable Medical Corp. | 1997 | — |
| −1 | K981219 | Oscar Bipolar Scissors and Oscar Bipolar Reusable Cartridges | Enable Medical Corp. | 1998 | — |
| 0 (this device) | K992996 | Enable Endoscopic Bipolar Scissors | Enable Medical Corp. | 1999 | — |
| +1 | K001330 | Sovereign Bipolar Instruments | Aesculap, Inc. | 2000 | — |
| +2 | K030890 | Switchblade | Snowden Pencer, Inc. | 2003 | — |
| +3 | K113407 | Snowden Pencer Laparoscopic Ergonomic Reposable Scissors | Carefusion 2200, Inc. | 2012 | — |
| +2 | K160393 | AdTec | Aesculap, Inc. | 2016 | — |
| +4 | K132232 | Mins Needlescopic Resposable Device System | Minilap Technologies | 2013 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1995 | 3 | 0 |
| 1996 | 1 | 0 |
| 1997 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2000 | 1 | 0 |
| 2003 | 1 | 0 |
| 2008 | 1 | 0 |
| 2012 | 2 | 0 |
| 2013 | 1 | 0 |
| 2016 | 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 GEI? 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 GEI device
- #1 K231790 The InMode System with the Morpheus8 Applicatorsscore 32.7 · 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? (7)
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 |
|---|---|---|---|
| * | K950286 | Symbiosis Bipolar ScissorsSummary page 1…10(k) process] Class IT ENABLE Endoscopic Bipolar Scissors Electrosurgical cutting and coagulation device and accessories 21CFR878.4400 1. Symbiosis Bipolar Scissors (K950286 and K951387) 2. Everest Medical Bipolar Scissors (K945975 and K955001) 3. CardioThoracic Systems MIDCAB/SVH Bipolar Scissors (K… | 1995 |
| * | K951387 | Symbiosis Bipolar ScissorsSummary page 1…s] Class IT ENABLE Endoscopic Bipolar Scissors Electrosurgical cutting and coagulation device and accessories 21CFR878.4400 1. Symbiosis Bipolar Scissors (K950286 and K951387) 2. Everest Medical Bipolar Scissors (K945975 and K955001) 3. CardioThoracic Systems MIDCAB/SVH Bipolar Scissors (K963930) 4.… | 1995 |
| * | K945975 | Evershears (R) Scissors, Bilap (R) Probes, Bicoag (R) ForcepsSummary page 1…Electrosurgical cutting and coagulation device and accessories 21CFR878.4400 1. Symbiosis Bipolar Scissors (K950286 and K951387) 2. Everest Medical Bipolar Scissors (K945975 and K955001) 3. CardioThoracic Systems MIDCAB/SVH Bipolar Scissors (K963930) 4. ENABLE Medical Corporation Bipolar Scissors (K9… | 1994 |
| * | K955001 | Evershears Scissors, Bilap Probes, Bicoag ForcepsSummary page 1…ical cutting and coagulation device and accessories 21CFR878.4400 1. Symbiosis Bipolar Scissors (K950286 and K951387) 2. Everest Medical Bipolar Scissors (K945975 and K955001) 3. CardioThoracic Systems MIDCAB/SVH Bipolar Scissors (K963930) 4. ENABLE Medical Corporation Bipolar Scissors (K972558 and K9… | 1995 |
| * | K963930 | CTS Midcab/SVH Bipolar ScissorsSummary page 1…0 1. Symbiosis Bipolar Scissors (K950286 and K951387) 2. Everest Medical Bipolar Scissors (K945975 and K955001) 3. CardioThoracic Systems MIDCAB/SVH Bipolar Scissors (K963930) 4. ENABLE Medical Corporation Bipolar Scissors (K972558 and K981219) INTENDED USE The ENABLE Endoscopic Bipolar Scissors inte… | 1997 |
| * | K972558 | Bipolar ScissorsSummary page 1…Everest Medical Bipolar Scissors (K945975 and K955001) 3. CardioThoracic Systems MIDCAB/SVH Bipolar Scissors (K963930) 4. ENABLE Medical Corporation Bipolar Scissors (K972558 and K981219) INTENDED USE The ENABLE Endoscopic Bipolar Scissors intended use is substantially equivalent to the intended use s… | 1997 |
| * | K981219 | Oscar Bipolar Scissors and Oscar Bipolar Reusable CartridgesSummary page 1…ical Bipolar Scissors (K945975 and K955001) 3. CardioThoracic Systems MIDCAB/SVH Bipolar Scissors (K963930) 4. ENABLE Medical Corporation Bipolar Scissors (K972558 and K981219) INTENDED USE The ENABLE Endoscopic Bipolar Scissors intended use is substantially equivalent to the intended use statements of… | 1998 |
What descends from it? (7)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K001330 | Sovereign Bipolar Instruments | 2000 | 6 |
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 5 years and passes through 2 companies; a new generation was cleared every 1.4 years on median.
- None of the 9 ancestors has a recall.
- Of its descendants, K001330 (Aesculap, Inc., 2000) has gone furthest, with 6 descendants of its own.
- 1 other device also cites its predicate K950286.
How does its category compare?
All GEI devicesGEI Electrosurgical, Cutting & Coagulation & Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · GEI
52in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · GEI
113in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GEI
4in 2025
Class I (14 since 2007) Class II/III not classified
Adverse event reports per year · GEI
7,592in 2025
MAUDE reports naming product code GEI, 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 | 50 | 51 | 21 | 2,795 |
| 2008 | 61 | 71 | 19 | 2,556 |
| 2009 | 42 | 130 | 27 | 3,591 |
| 2010 | 46 | 109 | 51 | 3,377 |
| 2011 | 35 | 135 | 32 | 4,463 |
| 2012 | 39 | 133 | 30 | 5,216 |
| 2013 | 48 | 136 | 13 | 4,897 |
| 2014 | 49 | 103 | 3 | 4,908 |
| 2015 | 47 | 123 | 4 | 4,936 |
| 2016 | 64 | 108 | 3 | 5,616 |
| 2017 | 52 | 72 | 2 | 6,073 |
| 2018 | 47 | 93 | 6 | 6,545 |
| 2019 | 48 | 93 | 5 | 7,067 |
| 2020 | 59 | 105 | 1 | 6,490 |
| 2021 | 46 | 146 | 6 | 6,354 |
| 2022 | 55 | 150 | 49 | 6,103 |
| 2023 | 65 | 104 | 27 (4) | 7,176 |
| 2024 | 59 | 125 | 22 (10) | 7,897 |
| 2025 | 52 | 113 | 4 | 7,592 |
| 2026 | 43 | 183 | 8 | — |
What is it indicated for?
The Enable Endoscopic Bipolar Scissors is intended to cut tissue and control bleeding through coagulation during laparoscopic and general surgical procedures.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K992996 · printed Nov 6, 2026
Cite this page
510(k) Report. “K992996: Enable Endoscopic Bipolar Scissors.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K992996
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