MaxBraid Suture BroadBand Tape (Ultra)
Subscapularis Repair Suture Kit-Ultra (Suture Kit - KIT701 is convenience kit containing HS Fiber sutures (K190817) and Drill Bit (HTW, 510k exempt)).
2manufacturers in China registered for this device type
1catalogue number
Who Else Makes It
Concentrated in Hubei (1), Zhejiang (1).
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Hubei Lanbin Medical Group Co., Ltd. | Xiaogan | Hubei | Contract manufacturer | 33 |
| Ningbo Greatcare Medical Instruments Co., Ltd. | Ningbo | Zhejiang | Contract manufacturer | 10 |
Record
| Listed by | Riverpoint Medical LLC, United States |
|---|---|
| FDA product code | OVN |
| Device type | Suture Kit |
| Device class | Class 2 |
| Regulation | 21 CFR 878.4830 |
| Establishment | Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer |
| Premarket notification | Exempt |
| Record published | 2022-07-27 |
| Record revised | 2026-05-19 (version 5) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date, manufacturing date |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 110046455 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Deknatel | Teleflex Medical LLC | 360 |
| Medical Action Industries | Medical Action Industries, Inc. | 326 |
| Syneture | Covidien LP | 321 |
| Cardinal Health | Cardinal Health 200, LLC | 220 |
| LSL Healthcare | Lsl Industries, Inc. | 41 |
| Medichoice | Owens & Minor Distribution, Inc. | 22 |
| Novaplus® | Medical Action Industries, Inc. | 20 |
| Medline Industries, Inc. | Medline Industries, Inc. | 8 |
| DeRoyal | Deroyal Industries, Inc. | 7 |
| Vygon | Vygon Corp. | 6 |
| ACS | American Contract Systems, Inc. | 5 |
| McKesson | Mckesson Medical-Surgical Inc. | 3 |
Showing 12 of 28. All products under Suture Kit
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.