# Nu-Tek Health (Hongkong) Limited (foreign exporter, Kowloon Bay, HK): 9 new FDA device listings, incl. interferential current therapy

**Score:** 55/100

| Field | Value |
|---|---|
| Establishment | Nu-Tek Health (Hongkong) Limited |
| Role | Foreign exporter |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device |
| Location | Kowloon Bay, HK |
| New listings | 9 |
| Devices | Interferential Current Therapy; Stimulator, Muscle, Powered; Device, Biofeedback; Stimulator, Nerve, Transcutaneous, For Pain Relief; Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat; Stimulator, Neuromuscular, External Functional; Lamp, Infrared, Therapeutic Heating; Massager, Therapeutic, Electric; Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat |
| Product codes | LIH, IPF, HCC, GZJ, IMG, GZI, ILY, ISA, IMJ |
| Device classes | Class I, Class II |
| Medical specialties | Neurology, Physical Medicine |
| First new listing | 2026-08-17 |
| Latest new listing | 2026-08-17 |
| FDA registration number | 3049809930 |
| Registration expires | 2026-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-11-04T21:52:36.524Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.