Catalogue number 0V52XX1011JK01, listed by Thermotek, Inc., United States, under Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat. 4 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 echoRx, Guide,quick Start,sngl,usnd | Listed by | Thermotek, Inc., United States |
| FDA product code | IMI |
| Device type | Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat |
| Device class | Class 2 |
| Regulation | 21 CFR 890.5300 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer |
| 510(k) | K240788 |
| Record published | 2026-02-23 |
Specifications
Specifications | MRI safety | MR Unsafe |
| Prescription | Prescription only |
| Label carries | manufacturing date |
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.