510(k) · Cleared
ClearedJewel Soft Tissue Reinforcement Device (102-6005)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Xiros Limited · QUW Mesh, Surgical, Non-Resorbable, Orthopedics, Reinforcement Of Ligament
Cleared on Jul 15, 2025 as substantially equivalent to K222978 (Xiros, Ltd., 2022) after a 350-day review. Its family tree reaches back 15 generations to 1993.
- Decided
- Jul 15, 2025
- Review
- 350 days
- Class
- Class II
- Product code
- QUW
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 15 generations to K931386 (1993). 94 ancestors in all, the oldest K810428 (1981). No later device cites it as a predicate yet.
- Root · 15 generations backK931386 Hemashield Microvel/Woven Double Velour FabricMeadox Medicals, Div. Boston Scientific Corp. · 1993
- 11 generations between
- 3 generations backK131143 Trellis Collagen RibbonWrightmedicaltechnologyinc · 2013
- 2 generations backK151083 BioBridge Collagen MatrixFibralign Corporation · 2016
- 1 generation backK222978 Poly-Tape/Infinity-Lock Soft Tissue Reinforcement DeviceXiros, Ltd. · 2022
- This deviceK242237 Jewel Soft Tissue Reinforcement Device (102-6005)Xiros Limited · 2025
Show all 15 generations
- Root · 15 generations backK931386 Hemashield Microvel/Woven Double Velour FabricMeadox Medicals, Div. Boston Scientific Corp. · 1993
- 14 generations backK963611 Vascutek Cardiovascular Fabric: Vascutek Gelseal Patch,Vascutek…Vascutek, Ltd. · 1996 · Recalled
- 13 generations backK972651 IN-SlingInfluence, Inc. · 1997
- 12 generations backK980482 Triangle SlingInfluence, Inc. · 1998
- 11 generations backK002721 Ams Triangle Silicone-Coated Sling and Surgical MeshAmerican Medical Systems, Inc. · 2000
- 10 generations backK010931 Ams Sacral Colpopexy Sling, Model 72403501American Medical Systems, Inc. · 2001
- 9 generations backK033636 Ams Large Pore Polypropylene MeshAmerican Medical Systems, Inc. · 2003
- 8 generations backK040521 Modification to Ams Large Pore Polypropylene MeshAmerican Medical Systems, Inc. · 2004
- 7 generations backK040623 Ams Perigee SystemAmerican Medical Systems, Inc. · 2004
- 6 generations backK050445 Ams Collagen Dermal MatrixAmerican Medical Systems, Inc. · 2005 · Recalled
- 5 generations backK073219 WMT Collagen Dermal Matrix, 4 CM X 7 CM, Model 89XM-4X07, VMT…American Medical Systems, Inc. · 2008
- 4 generations backK120019 Collagen RibbonWrightmedicaltechnologyinc · 2012
- 3 generations backK131143 Trellis Collagen RibbonWrightmedicaltechnologyinc · 2013
- 2 generations backK151083 BioBridge Collagen MatrixFibralign Corporation · 2016
- 1 generation backK222978 Poly-Tape/Infinity-Lock Soft Tissue Reinforcement DeviceXiros, Ltd. · 2022
- This deviceK242237 Jewel Soft Tissue Reinforcement Device (102-6005)Xiros Limited · 2025
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −15 | K931386 | Hemashield Microvel/Woven Double Velour Fabric | Meadox Medicals, Div. Boston Scientific Corp. | 1993 | — |
| −14 | K963611 | Vascutek Cardiovascular Fabric: Vascutek Gelseal Patch,Vascutek Gelsoft… | Vascutek, Ltd. | 1996 | 1 |
| −13 | K972651 | IN-Sling | Influence, Inc. | 1997 | — |
| −12 | K980482 | Triangle Sling | Influence, Inc. | 1998 | — |
| −11 | K002721 | Ams Triangle Silicone-Coated Sling and Surgical Mesh | American Medical Systems, Inc. | 2000 | — |
| −10 | K010931 | Ams Sacral Colpopexy Sling, Model 72403501 | American Medical Systems, Inc. | 2001 | — |
| −9 | K033636 | Ams Large Pore Polypropylene Mesh | American Medical Systems, Inc. | 2003 | — |
| −8 | K040521 | Modification to Ams Large Pore Polypropylene Mesh | American Medical Systems, Inc. | 2004 | — |
| −7 | K040623 | Ams Perigee System | American Medical Systems, Inc. | 2004 | — |
| −6 | K050445 | Ams Collagen Dermal Matrix | American Medical Systems, Inc. | 2005 | 1 |
| −5 | K073219 | WMT Collagen Dermal Matrix, 4 CM X 7 CM, Model 89XM-4X07, VMT Collagen Dermal… | American Medical Systems, Inc. | 2008 | — |
| −4 | K120019 | Collagen Ribbon | Wrightmedicaltechnologyinc | 2012 | — |
| −3 | K131143 | Trellis Collagen Ribbon | Wrightmedicaltechnologyinc | 2013 | — |
| −2 | K151083 | BioBridge Collagen Matrix | Fibralign Corporation | 2016 | — |
| −1 | K222978 | Poly-Tape/Infinity-Lock Soft Tissue Reinforcement Device | Xiros, Ltd. | 2022 | — |
| 0 (this device) | K242237 | Jewel Soft Tissue Reinforcement Device (102-6005) | Xiros Limited | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1981 | 1 | 0 |
| 1983 | 1 | 0 |
| 1985 | 1 | 0 |
| 1988 | 1 | 0 |
| 1991 | 3 | 0 |
| 1992 | 4 | 0 |
| 1993 | 2 | 0 |
| 1994 | 2 | 0 |
| 1996 | 8 | 0 |
| 1997 | 4 | 0 |
| 1998 | 8 | 0 |
| 1999 | 2 | 0 |
| 2000 | 9 | 0 |
| 2001 | 5 | 0 |
| 2002 | 9 | 0 |
| 2003 | 5 | 0 |
| 2004 | 6 | 0 |
| 2005 | 2 | 0 |
| 2006 | 1 | 0 |
| 2007 | 3 | 0 |
| 2008 | 1 | 0 |
| 2014 | 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 QUW? 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 QUW device
- #1 K251063 TekBrace Solo Soft Tissue Reinforcement Devicescore 19.6 · 15 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 |
|---|---|---|---|
| * | K222978 | Poly-Tape/Infinity-Lock Soft Tissue Reinforcement DeviceSummary page 5…inforcement Device described in this premarket submission is substantially equivalent to the following device: Poly-Tape/Infinity-Lock Soft Tissue Reinforcement Device (K222978) – Primary Predicate Device Device Description: The Jewel Soft Tissue Reinforcement Device is a woven tubular implantable devic… | 2022 |
What descends from it?
No later submission names this one as a predicate yet.
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 32 years and passes through 8 companies; a new generation was cleared every 2.3 years on median.
- 8 of the 94 ancestors have a recall of any class.
- 2 other devices also cite its predicate K222978.
How does its category compare?
All QUW devicesQUW Mesh, Surgical, Non-Resorbable, Orthopedics, Reinforcement Of Ligament: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.
FDA decisions per year · QUW
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · QUW
Too few QUW 510(k)s in any year since 2007 to give a median.
Recalls per year · QUW
No recall names QUW since 2007.
Adverse event reports per year · QUW
No MAUDE report names QUW since 2007.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 1 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 2 | — | 0 | 0 |
| 2026 | 2 | — | 0 | — |
What is it indicated for?
The Jewel Soft Tissue Reinforcement Device is a single-use device intended for reinforcement of soft tissues that are undergoing reconstruction surgery, utilizing autograft or allograft soft tissue grafts, or are to be repaired by suture or other fixation devices during ligament repair surgery. This includes reinforcement of extra-articular ligaments such as, but not limited to, medial collateral ligament, lateral collateral ligament, spring ligament…
Read the full statement (130 words)
The Jewel Soft Tissue Reinforcement Device is a single-use device intended for reinforcement of soft tissues that are undergoing reconstruction surgery, utilizing autograft or allograft soft tissue grafts, or are to be repaired by suture or other fixation devices during ligament repair surgery. This includes reinforcement of extra-articular ligaments such as, but not limited to, medial collateral ligament, lateral collateral ligament, spring ligament, deltoid ligament, and ulnar collateral ligament.
The Jewel Soft Tissue Reinforcement Device is not intended to replace normal body structure or provide the full mechanical strength to support the medial collateral ligament, lateral collateral ligament, spring ligament, deltoid ligament, ulnar collateral ligament or other extra-articular ligaments. Sutures, or other fixation devices, used to attach the tissue to the bone, provide mechanical strength for the reconstruction or repair.
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/K242237 · printed Nov 5, 2026
Cite this page
510(k) Report. “K242237: Jewel Soft Tissue Reinforcement Device (102-6005).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K242237
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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