Axonics
Curved Charging Belt - Extended
1manufacturer
22catalogue numbers in this listing
Who Else Makes It
Registered in Shanghai.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Jabil Circuit (Shanghai) Ltd. | Shanghai | Shanghai | Contract manufacturer | 31 |
Record
| Listed by | Axonics Modulation Technologies, Inc. |
|---|---|
| FDA product code | QON |
| Device type | Implanted Electrical Device Intended For Treatment Of Fecal Incontinence |
| Device class | Class 3 |
| Regulation | 21 CFR 876.5270 |
| Record published | 2019-09-23 |
| Record revised | 2026-05-18 (version 7) |
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, manufacturing date, serial number |
Catalogue Numbers
| Catalogue number | Size | Per pack | Status |
|---|---|---|---|
| 9008-R | In distribution | ||
| 9004 | 10 | In distribution | |
| 2301 | In distribution | ||
| 1401 | In distribution | ||
| 9014 | 4 | In distribution | |
| 9108-E | In distribution | ||
| 9005 | 9 | In distribution | |
| 9007 | 6 | In distribution | |
| 9003 | 6 | In distribution | |
| 2201 | In distribution | ||
| 9009 | In distribution | ||
| 1801 | In distribution | ||
| 1701 | In distribution | ||
| 9006 | 6 | In distribution | |
| 9015 | 2 | In distribution | |
| 2501 | In distribution | ||
| 9011 | 6 | In distribution | |
| 1601 | In distribution | ||
| 1401 | In distribution | ||
| 1201 | In distribution | ||
| 1401 | In distribution | ||
| 1901 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Implanted Electrical Device Intended For Treatment Of Fecal Incontinence | Medtronic, Inc. | 6 |
| InterStim™ SureScan™ | Medtronic, Inc. | 5 |
| Verify™ | Medtronic, Inc. | 4 |
| InterStim™ X | Medtronic, Inc. | 1 |
| InterStim™ Micro SureScan™ MRI | Medtronic, Inc. | 1 |
| Interstim® II | Medtronic, Inc. | 1 |
PMA Approvals
A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.
| PMA number | Decision | Trade name | Approved to |
|---|---|---|---|
| P080025 | 2024-12-13 | InterStim Therapy System, Verify Evaluation System | Medtronic Neuromodulation |
| P190006 | 2023-03-02 | Axonics Sacral Neuromodulation System | Boston Scientific Corporation |
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.