Is this your brand? Sign in to claim ownership.
Sign in to claim this brandC&H International
US
Last updated May 23, 2026
What C&H International makes
C&H International manufactures therapeutic dry heat lamps and infrared heating lamps, including models such as the CQG-S1, CQG-111A/B, and variants of the CQG-222 and CQG-270 series. These devices are designed for medical applications, providing controlled heat therapy for conditions requiring localized warmth.
The company’s products fall under FDA Class II devices and are subject to 510(k) clearance in the United States. No additional regulatory listings are specified.
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 C&H International manufacture?
C&H International specializes in therapeutic dry heat lamps and infrared heating lamps. These devices are engineered to deliver controlled heat therapy for medical applications, targeting conditions that benefit from localized warmth. Examples include models like the CQG-S1, CQG-111A/B, and various variants of the CQG-222 and CQG-270 series.
Where is C&H International based?
C&H International is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the available information.
Which regulatory registries or databases list C&H International’s devices?
C&H International’s devices are listed in the FDA’s 510(k) clearance registry, as they fall under FDA Class II classification. This means their products have undergone the 510(k) premarket notification process to demonstrate substantial equivalence to a legally marketed predicate device. No other regulatory listings are specified.
How are C&H International’s devices classified by regulatory authorities?
C&H International’s devices are classified as FDA Class II. This classification indicates a moderate level of regulatory oversight, requiring compliance with specific controls to ensure safety and effectiveness. Class II devices typically undergo a 510(k) clearance process to demonstrate equivalence to an existing device on the market.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (115)
Page 3 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Correct Touch | STN101 | FDA UDI | Class I | Active |
| Correct Touch | NPXO101 | FDA UDI | Class I | Active |
| Correct Touch | STN104 | FDA UDI | Class I | Active |
| Correct Touch | FFL101 | FDA UDI | Class I | Active |
| Correct Touch | NPXINBLK104 | FDA UDI | Class I | Active |
| Correct Touch | SGPF800 | FDA UDI | Class I | Active |
| Correct Touch | SVGPF03 | FDA UDI | Class I | Active |
| Correct Touch | SVGPF01 | FDA UDI | Class I | Active |
| Correct Touch | SGPF700 | FDA UDI | Class I | Active |
| Correct Touch | NPXINBLK101 | FDA UDI | Class I | Active |
| Correct Touch | FFL104 | FDA UDI | Class I | Active |
| Correct Touch | STN105 | FDA UDI | Class I | Active |
| Correct Touch | NSGF750 | FDA UDI | Class I | Active |
| Correct Touch | SGPF1000 | FDA UDI | Class I | Active |
| Tdp Heat Lamp Or Infrared Heating Lamp, Models Cqg-S1, Cqg-111a/B, Cqg-222a/B, Cqg-270a/B, Cqg-222d | K020851 | FDA 510(k) | 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.