510(k) · Cleared
ClearedPowergrip Bipolar Coagulation Forceps, Model 824XXXXX
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Gunter Bissinger Medizintechnik GmbH · HET Laparoscope, Gynecologic (And Accessories)
Cleared on Mar 11, 2004 as substantially equivalent to K970968 (Guenter Bissinger Medizintechnik GmbH, 1998) after a 162-day review. Its family tree reaches back 1 generation to 1998. 1 later device descends from it.
- Decided
- Mar 11, 2004
- Review
- 162 days
- Class
- Class II
- Product code
- HET
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K970968 (1998). 1 later device descends from it, 1 citing it directly.
- Root · 1 generation backK970968 Bissinger Detachable Bipolar Coagulation-ForcepsGuenter Bissinger Medizintechnik GmbH · 1998
- This deviceK033177 Powergrip Bipolar Coagulation Forceps, Model 824XXXXXGunter Bissinger Medizintechnik GmbH · 2004
- Descendant · cites it directly · 0 of its ownK082505 KLS Martin Electrosurgical InstrumentsKl Martin L.P. · 2009
Most influential descendants
Showing 1 of 1 · See all- K082505KLS Martin Electrosurgical InstrumentsKl Martin L.P. · 2009 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K970968 | Bissinger Detachable Bipolar Coagulation-Forceps | Guenter Bissinger Medizintechnik GmbH | 1998 | — |
| 0 (this device) | K033177 | Powergrip Bipolar Coagulation Forceps, Model 824XXXXX | Gunter Bissinger Medizintechnik GmbH | 2004 | — |
| +1 | K082505 | KLS Martin Electrosurgical Instruments | Kl Martin L.P. | 2009 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2009 | 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 HET? 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 HET device
- #1 K250939 SIRIUS Endoscope System (PR-SI-1230)score 12.9 · 11 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 |
|---|---|---|---|
| * | K970968 | Bissinger Detachable Bipolar Coagulation-ForcepsSummary page 1…Change in control mechanism of forceps jaws 2.6 Modification to Existing Device: [807.92 (a)(3)] K 970968 Bissinger Detachable Bipolar Coagulation Forceps (Cleared 05/21/98… | 1998 |
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 |
|---|---|---|---|
| K082505 | KLS Martin Electrosurgical Instruments | 2009 | 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?
How does its category compare?
All HET devicesHET Laparoscope, Gynecologic (And Accessories): FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · HET
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · HET
269in 2021
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · HET
4in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · HET
4,513in 2025
MAUDE reports naming product code HET, 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 | 0 | — | 0 | 181 |
| 2008 | 3 | 176 | 4 | 359 |
| 2009 | 1 | — | 1 | 403 |
| 2010 | 1 | — | 0 | 214 |
| 2011 | 2 | — | 0 | 417 |
| 2012 | 2 | — | 0 | 1,118 |
| 2013 | 2 | — | 0 | 1,035 |
| 2014 | 0 | — | 0 | 175 |
| 2015 | 2 | — | 1 | 124 |
| 2016 | 0 | — | 0 | 205 |
| 2017 | 2 | — | 0 | 89 |
| 2018 | 1 | — | 0 | 53 |
| 2019 | 2 | — | 0 | 44 |
| 2020 | 2 | — | 0 | 49 |
| 2021 | 4 | 269 | 0 | 132 |
| 2022 | 1 | — | 1 | 216 |
| 2023 | 0 | — | 4 | 824 |
| 2024 | 0 | — | 0 | 3,496 |
| 2025 | 2 | — | 0 | 4,513 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
Bipolar tissue coagulation in gynecologic and laparoscopic 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/K033177 · printed Nov 3, 2026
Cite this page
510(k) Report. “K033177: Powergrip Bipolar Coagulation Forceps, Model 824XXXXX.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K033177
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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