OC JuggerLoop™ Soft Anchor
The OC JuggerLoop Soft Anchor is an implant for fixing soft tissue to bone in orthopedic procedures. Its suture sleeve structure works with shuttling and cinching sutures to support the…
The OC JuggerLoop Soft Anchor is an implant for fixing soft tissue to bone in orthopedic procedures. Its suture sleeve structure works with shuttling and cinching sutures to support the fixation arrangement. It is intended for hospital, clinic or surgical use.
The anchor sleeve is made from nonabsorbable braided polyester, with nonabsorbable braided UHMWPE sutures spliced through it. Hydroxyapatite and bioceramic particles are embedded in the surface of the anchor material.
Procedure Scope and Supply
Applications include specified knee tendon and ligament repairs, foot and ankle repairs, rotator cuff and shoulder instability procedures, biceps tenodesis and elbow tendon repair or reattachment. The device is supplied sterile after ethylene oxide sterilization for single use.
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) | K243203 |
| Record published | 2024-12-19 |
Specifications
| MRI safety | MR Safe |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Label carries | lot or batch number, expiry date, manufacturing date |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 120003961 | In distribution | |
| 120003962 | In distribution | |
| 120003960 | 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.