4 catalogue numbers from A400, listed by Zylox-Tonbridge Medical Technology Co., Ltd., under Catheter, Peripheral, Atherectomy. 3 manufacturers in China are registered for this product code.
Who Else Makes It
All of them in Guangdong. 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
Record
Regulatory record for Pantheris | Listed by | Zylox-Tonbridge Medical Technology Co., Ltd. |
| FDA product code | MCW |
| Device type | Catheter, Peripheral, Atherectomy |
| Device class | Class 2 |
| Regulation | 21 CFR 870.4875 |
| Record published | 2026-03-21 |
| Record revised | 2026-07-28 (version 2) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Supplied sterile | Yes |
| Single use | Yes |
| Label carries | lot or batch number, expiry date, manufacturing date |
| Distribution end date | 2026-07-24 |
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.