RootMend™ MRR (Blue)
RootMend MRR is an adjustable suture-loop device used to secure soft tissue to bone during meniscal root repair in the knee. The listed version uses blue suture material. The loop works…
RootMend MRR is an adjustable suture-loop device used to secure soft tissue to bone during meniscal root repair in the knee. The listed version uses blue suture material. The loop works with a fixation button to hold the repair at the bone.
The suture component is uncoated ultra-high molecular weight polyethylene with tracer filaments. The system offers fixation buttons made from titanium alloy or suture material. The appropriate fixation configuration is selected as part of the repair construct.
Sterile Supply
RootMend MRR is supplied sterile following ethylene oxide sterilization for a single use. It must not be resterilized.
Who Else Makes It
Concentrated in Jiangsu (3), Shanghai (2), Zhejiang (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Suzhou Elite Precision Machinery Co., Ltd. | Kunshan | Jiangsu | Contract manufacturer | 35 |
| Suzhou Kangli Orthopaedics Instrument Co., Ltd. | Zhangjiagang | Jiangsu | Contract manufacturer | 11 |
| Renolit Hansen Packaging Tech. (BJ) Ltd. | Beijing | Beijing | Contract manufacturer | 1 |
| Zimmer (Shanghai) Medical International Trading Co., Ltd. | Shanghai | Shanghai | Exporter | 106 |
| Arthrex (Shanghai) Co., Ltd. | Shanghai | Shanghai | Exporter | 38 |
| Suzhou Endophix Co., Ltd. | Suzhou | Jiangsu | Manufacturer | 17 |
| Zhejiang Decans Medical Devices Co., Ltd. | Jiaxing | Zhejiang | Manufacturer | 10 |
Record
| Listed by | Riverpoint Medical LLC, United States |
|---|---|
| FDA product code | MBI |
| Device type | Fastener, Fixation, Nondegradable, Soft Tissue |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3040 |
| Establishment | Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer |
| 510(k) | K243988 |
| Record published | 2025-05-01 |
Specifications
| MRI safety | MR Conditional |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Label carries | lot or batch number, expiry date, manufacturing date |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 110.000 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Arthrex® | Arthrex, Inc. | 362 |
| HNM Sports Medicine | HNM Stainless, LLC. | 150 |
| Suture Anchors – HTA Headless Titanium Anchor and Zip Anchors | GM DOS Reis Industria E Comercio Ltda | 78 |
| Juggerknot® | Biomet Orthopedics | 77 |
| Fastener, Fixation, Nondegradable, Soft Tissue | Parcus Medical, LLC | 74 |
| endophix | Suzhou Endophix Co., Ltd. | 71 |
| Titan | Medline Industries, Inc. | 68 |
| TopLock | Fusion Orthopedics, LLC | 67 |
| HNM Medical | HNM Stainless, LLC. | 59 |
| Orthobutton CL | Riverpoint Medical LLC | 55 |
| Apollo | Medline Industries, Inc. | 53 |
| JuggerKnot Soft Anchor | Riverpoint Medical LLC | 46 |
Showing 12 of 618. All products under Fastener, Fixation, Nondegradable, Soft Tissue
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K262677 | 2026-08-27 |
| K253693 | 2026-03-11 |
| K253695 | 2026-02-27 |
| K252144 | 2025-07-30 |
| K243988 | 2025-03-20 |
| K242494 | 2024-11-26 |
| K243323 | 2024-11-19 |
| K243203 | 2024-10-29 |
| K241577 | 2024-07-03 |
| K240719 | 2024-04-11 |
| K240213 | 2024-02-23 |
| K240194 | 2024-02-21 |
| K233552 | 2023-11-30 |
| K233468 | 2023-11-14 |
| K232411 | 2023-10-06 |
| K231078 | 2023-10-05 |
| K231278 | 2023-08-01 |
| K231128 | 2023-05-17 |
| K230212 | 2023-02-23 |
| K203740 | 2021-02-12 |
| K202399 | 2020-09-18 |
| K171060 | 2017-06-02 |
| K160655 | 2016-06-03 |
Recalls
1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|
| 2023-10-25 | Class II | Component design/selection | Use of a 1.4 drill in hard bone conditions caused increased insertion forces leading to subsequent failures of the inserter, when the inserters bend, it may also move off the drill hole location leading to damage of the suture construct dur | 999 devices |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.