Is this your brand? Sign in to claim ownership.
Sign in to claim this brandHTK ENTERPRISES, INC.
US
Last updated May 24, 2026
What HTK ENTERPRISES, INC. makes
HTK Enterprises, Inc. manufactures physical therapy devices designed for transcutaneous neuromuscular electrical stimulation (TENS/NMES). Their portfolio includes the InterX system, which delivers targeted electrical stimulation for muscle re-education and rehabilitation purposes.
The company’s devices fall under FDA Class II regulation and are listed in the FDA’s Unique Device Identifier (UDI) database. HTK Enterprises, Inc. is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does HTK Enterprises, Inc. manufacture?
HTK Enterprises, Inc. specializes in physical therapy devices, specifically transcutaneous neuromuscular electrical stimulation (TENS/NMES) systems. These devices are designed to deliver controlled electrical impulses to muscles through the skin, aiding in muscle re-education and rehabilitation. The primary focus is on devices like the InterX system, which targets neuromuscular stimulation for therapeutic purposes.
Where is HTK Enterprises, Inc. based?
HTK Enterprises, Inc. is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework, as it operates under U.S. medical device regulations, including FDA requirements.
Which regulatory registries or databases list HTK Enterprises, Inc.’s devices?
HTK Enterprises, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the supply chain, allowing healthcare providers and regulators to verify device details, such as manufacturer information and classification.
How are HTK Enterprises, Inc.’s devices classified under U.S. regulations?
HTK Enterprises, Inc.’s devices fall under FDA Class II classification. This classification is assigned based on the risk associated with the device—Class II devices generally pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness, such as performance standards or post-market surveillance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- interx.com
- —
- —
- [email protected]
- Phone
- 972-665-1810
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 056903080
Catalogue (17)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| InterX | 533 | FDA UDI | Class II | Active |
| InterX | 500 | FDA UDI | Class II | Active |
| InterX | 1507 | FDA UDI | Class II | Active |
| InterX | 150U | FDA UDI | Class II | Active |
| InterX | 5002 | FDA UDI | Class II | Active |
| InterX | 1475 | FDA UDI | Class II | Active |
| InterX | Personal Sport | FDA UDI | Class II | Active |
| InterX | 900 | FDA UDI | Class II | Active |
| InterX | 1589 | FDA UDI | Class II | Active |
| InterX | 300 | FDA UDI | Class II | Active |
| InterX | Professional Sport | FDA UDI | Class II | Active |
| InterX | 350U | FDA UDI | Class II | Active |
| InterX | 1000 | FDA UDI | Class II | Active |
| InterX | 200 | FDA UDI | Class II | Active |
| InterX | 400 | FDA UDI | Class II | Active |
| InterX | 250 | FDA UDI | Class II | Active |
| InterX | 1675 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.