510(k) · Cleared
ClearedAllis Tissue Forceps, 4X5 Teeth, 6+SS 410 or 420
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
The Huxley Instrument Corp. · KOA Surgical Instruments, G-U, Manual (And Accessories)
Cleared on Jul 9, 1985 after a 13-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 6 later devices descend from it.
- Decided
- Jul 9, 1985
- Review
- 13 days
- Class
- Class I
- Product code
- KOA
- Recalls
- None
- Predicates
- 0
6 later devices descend from it, 1 citing it directly.
- This deviceK852726 Allis Tissue Forceps, 4X5 Teeth, 6+SS 410 or 420The Huxley Instrument Corp. · 1985
- Descendant · cites it directly · 5 of its ownK061387 Veresure BellVeresure, Inc. · 2006
- Descendant · 2 generations on · 4 of its ownK070651 Aragon Surgical LapcapAragon Surgical, Inc. · 2007
- Descendant · 3 generations on · 1 of its ownK233020 TauTona Pneumoperitoneum Assist Device (TPAD)Tautona Group Research & Development, Co., LLC · 2024
- Descendant · 3 generations on · 1 of its ownK073452 Modification to: Aragon Surgical LapcapAragon Surgical, Inc. · 2008
- Descendant · 4 generations on · 0 of its ownK242536 TauTona Pneumoperitoneum Assist Device (TPAD)Tautona Group · 2024
Showing 5 of 6 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 6 · See all- K061387Veresure BellVeresure, Inc. · 2006 · cites it directly5descendants
- K070651Aragon Surgical LapcapAragon Surgical, Inc. · 2007 · 2 generations on4descendants
- K233020TauTona Pneumoperitoneum Assist Device (TPAD)Tautona Group Research & Development, Co., LLC · 2024 · 3 generations on1descendant
- K073452Modification to: Aragon Surgical LapcapAragon Surgical, Inc. · 2008 · 3 generations on1descendant
- K242536TauTona Pneumoperitoneum Assist Device (TPAD)Tautona Group · 2024 · 4 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K852726 | Allis Tissue Forceps, 4X5 Teeth, 6+SS 410 or 420 | The Huxley Instrument Corp. | 1985 | — |
| +1 | K061387 | Veresure Bell | Veresure, Inc. | 2006 | — |
| +2 | K070651 | Aragon Surgical Lapcap | Aragon Surgical, Inc. | 2007 | — |
| +3 | K233020 | TauTona Pneumoperitoneum Assist Device (TPAD) | Tautona Group Research & Development, Co., LLC | 2024 | — |
| +3 | K073452 | Modification to: Aragon Surgical Lapcap | Aragon Surgical, Inc. | 2008 | — |
| +4 | K242536 | TauTona Pneumoperitoneum Assist Device (TPAD) | Tautona Group | 2024 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2006 | 1 | 0 |
| 2007 | 1 | 0 |
| 2008 | 1 | 0 |
| 2022 | 1 | 0 |
| 2024 | 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.
Planning a device in KOA? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin 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? (6)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K061387 | Veresure Bell | 2006 | 5 |
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?
- Of its descendants, K061387 (Veresure, Inc., 2006) has gone furthest, with 5 descendants of its own.
How does its category compare?
All KOA devicesKOA Surgical Instruments, G-U, Manual (And Accessories): FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · KOA
1in 2018
2026 to Oct 25, outlined.
Median 510(k) review, days · KOA
Too few KOA 510(k)s in any year since 2007 to give a median.
Recalls per year · KOA
No recall names KOA since 2007.
Adverse event reports per year · KOA
3in 2025
MAUDE reports naming product code KOA, 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 | 1 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 1 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 1 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 2 |
| 2017 | 0 | — | 0 | 3 |
| 2018 | 1 | — | 0 | 3 |
| 2019 | 0 | — | 0 | 2 |
| 2020 | 0 | — | 0 | 1 |
| 2021 | 0 | — | 0 | 1 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 5 |
| 2024 | 0 | — | 0 | 2 |
| 2025 | 0 | — | 0 | 3 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/K852726 · printed Nov 6, 2026
Cite this page
510(k) Report. “K852726: Allis Tissue Forceps, 4X5 Teeth, 6+SS 410 or 420.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K852726
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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