Argo Knotless Genesys
4.75mm Argo Knotless® GENESYSTM SP Anchor
7manufacturers in China registered for this device type
3catalogue numbers in this listing
16510(k) clearances naming this product code
1recall
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 | ConMed Corporation, 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, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K240090 |
| Record published | 2024-07-22 |
Specifications
| MRI safety | MR Conditional |
|---|---|
| Sterilisation | Ethylene Oxide |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Storage | Storage environment temperature 0 to 104 °F; Storage environment temperature 0 to 40 °C |
| Packaging | Carton |
| Sizes | Outer diameter 4.75 to 5.5 mm; outer diameter 0.187 to 0.217 in |
| Distribution end date | 2024-07-10 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| SPKBC55 | Outer Diameter 5.5 mm | In distribution |
| SPKBC475 | Outer Diameter 0.187 in | In distribution |
| SPKBC475 | Withdrawn |
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 |
|---|---|
| K261363 | 2026-05-13 |
| K253763 | 2026-01-29 |
| K251530 | 2025-06-18 |
| K244025 | 2025-01-28 |
| K220757 | 2022-05-13 |
| K193606 | 2020-01-22 |
| K191204 | 2019-07-03 |
| K190333 | 2019-03-18 |
| K182439 | 2019-01-08 |
| K182621 | 2019-01-04 |
| K181120 | 2018-12-21 |
| K182446 | 2018-12-19 |
| K171725 | 2017-09-08 |
| K163258 | 2017-01-25 |
| K151037 | 2015-07-09 |
| K133224 | 2014-01-03 |
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 | Closed |
|---|---|---|---|---|---|
| 2017-04-17 | Class II | Mixed-up of materials/components | Manufactured with the incorrect anchor outer body | 56 units | 2021-08-31 |
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.