Bard® InLay® Versa Fit® Ureteral Stent With HydroGlide™ Guidewire
Inlay Versa FIT Ureteral Stent W/Hydroglide Guidewire
4manufacturers in China registered for this device type
4catalogue numbers in this listing
7510(k) clearances naming this product code
8recalls on this code
Who Else Makes It
Concentrated in Shanghai (2), Zhejiang (1), Guangdong (1).
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Zhejiang Chuangxiang Medical Technology Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 27 |
| Alton Shanghai Medical Instruments Co Ltd | Shanghai | Shanghai | Complaint-file establishment | 20 |
| BQ Plus Medical Co., Ltd. | Songjiang | Shanghai | Contract manufacturer | 13 |
| Shenzhen Trious Medical Technology Co., Ltd. | Shenzhen | Guangdong | Manufacturer | 6 |
Record
| Listed by | C.R. Bard, Inc., United States |
|---|---|
| FDA product code | FAD |
| Device type | Stent, Ureteral |
| Device class | Class 2 |
| Regulation | 21 CFR 876.4620 |
| Establishment | Contract manufacturer, Contract steriliser, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| Record published | 2015-05-14 |
| Record revised | 2018-03-29 (version 2) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date |
| Sizes | Catheter gauge 4.7 to 8 Fr |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 777800 | Catheter Gauge 8 Fr | In distribution |
| 777400 | Catheter Gauge 4.7 Fr | In distribution |
| 777700 | Catheter Gauge 7 Fr | In distribution |
| 777600 | Catheter Gauge 6 Fr | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Porges Coloplast | Coloplast A/S | 509 |
| Polaris™ Ultra | Boston Scientific Corporation | 406 |
| Universa | Cook Incorporated | 384 |
| Percuflex™ Plus | Boston Scientific Corporation | 300 |
| Polaris™ Loop | Boston Scientific Corporation | 232 |
| ImaJin | Coloplast A/S | 219 |
| Contour™ | Boston Scientific Corporation | 205 |
| Percuflex™ | Boston Scientific Corporation | 152 |
| Tecoflex | Gyrus Acmi, Inc. | 92 |
| Vortek | Coloplast A/S | 92 |
| Sof-Flex | Cook Incorporated | 60 |
| Tria™ Firm | Boston Scientific Corporation | 58 |
Showing 12 of 131. All products under Stent, Ureteral
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K043193 | 2004-12-07 |
| K022447 | 2003-01-23 |
| K983498 | 1998-12-15 |
| K903345 | 1991-04-30 |
| K883561 | 1988-11-15 |
| K861478 | 1986-05-15 |
| K823487 | 1983-05-27 |
Recalls
8 of these are 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 |
|---|---|---|---|---|---|
| 2025-11-06 | Class II | Under Investigation by firm | Labeling discrepancy; Ureteral stent actual size may not match the actual product label. | 4350 units | |
| 2025-11-06 | Class II | Under Investigation by firm | Labeling discrepancy; Ureteral stent actual size may not match the actual product label. | 116 units | |
| 2025-11-06 | Class II | Under Investigation by firm | Labeling discrepancy; Ureteral stent actual size may not match the actual product label. | 116 units | |
| 2025-11-06 | Class II | Under Investigation by firm | Labeling discrepancy; Ureteral stent actual size may not match the actual product label. | 116 units | |
| 2016-10-13 | Class II | Labeling Change Control | Labeling: Statement was added to the Warnings/Precautions section requesting end users to consider the presence of a knot if significant resistance is encountered during attempts at removal. | 75,089 units | 2022-02-10 |
| 2016-10-13 | Class II | Labeling Change Control | Labeling: Statement was added to the Warnings/Precautions section requesting end users to consider the presence of a knot if significant resistance is encountered during attempts at removal. | 75,089 units | 2022-02-10 |
| 2016-10-13 | Class II | Labeling Change Control | Labeling: Statement was added to the Warnings/Precautions section requesting end users to consider the presence of a knot if significant resistance is encountered during attempts at removal. | 75,089 units | 2022-02-10 |
| 2016-10-13 | Class II | Labeling Change Control | Labeling: Statement was added to the Warnings/Precautions section requesting end users to consider the presence of a knot if significant resistance is encountered during attempts at removal. | 75,089 units | 2022-02-10 |
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.