It is a wrist-type low-level (cold) laser therapy device (model GD07-W-2, marketed as a 650nm Wrist Type Laser Therapy Watch) classified by the manufacturer as a Class II instrument, designed to provide non-invasive photobiomodulation to assist in rehabilitation and management of certain chronic conditions.
The device emits low‑level 650 nm laser light to penetrate superficial tissues and stimulate cellular activity and microcirculation. It is intended to support recovery processes and symptom management (as an adjunct), rather than serve as a stand-alone cure.
According to the manufacturer, it is intended to assist with hypertension and high blood lipids, help manage high blood sugar/diabetes, support recovery from cerebrovascular conditions such as stroke, and may be used to help manage symptoms related to rhinitis and nasal polyps. Use should be guided by a healthcare professional.
It is intended for adults receiving rehabilitation care (clinical or at home), patients recovering from stroke, and people with certain chronic conditions seeking adjunctive non-invasive therapy. Use in children should be under medical supervision.
No. This device is meant to be an adjunctive therapy. It should not replace prescribed medications or medically indicated treatments. Always consult your physician before changing or stopping any treatment.
The watch is worn on the wrist as instructed in the user manual. Typical low‑level laser therapy protocols are often in the range of 10–30 minutes per session, once or twice daily, but actual duration and frequency should follow the device manual or your healthcare provider's guidance.
Most users tolerate low‑level laser therapy well. Possible effects include mild skin redness, temporary warmth, local irritation, or photosensitivity. If you experience pain, worsening symptoms, dizziness, or other concerning reactions, stop use and consult your healthcare provider.
Avoid direct exposure to the eyes. Use caution and consult a physician before use if you are pregnant, have an active malignancy, implanted electronic devices (e.g., pacemaker), epilepsy, open wounds at the treatment site, or other serious medical conditions. Follow clinician advice for children.
The product description lists the instrument classification as Class II, but it does not specify regional regulatory approvals. Contact the manufacturer or seller for documentation of CE marking, FDA clearance, or other local regulatory certifications before purchase/use.
The device is described as suitable for both clinical and home use. However, home use should follow the user manual and any recommendations from your healthcare provider to ensure safe and effective application.
Results vary by individual, condition severity, and consistency of use. Some users may notice changes in weeks, while others may require longer-term therapy. Discuss realistic expectations and monitoring with your healthcare provider.
Single package dimensions are 16.5 x 16.5 x 8 cm, single gross weight is approximately 1.000 kg, and minimum order quantity is 1 piece.
Clean external surfaces with a soft, slightly damp cloth and mild detergent if needed. Do not immerse the device in water or use aggressive solvents. Power off and disconnect any power source before cleaning. Store in a cool, dry place when not in use.
Stop using the device immediately, consult your healthcare provider about any medical concerns, and contact the seller or manufacturer for technical support, repair, or warranty service. Keep purchase and device information (model GD07-W-2) handy when contacting support.
Contact the supplier or manufacturer for pricing, shipping options, certification documents, user manual, warranty terms, and bulk purchase inquiries. Provide the model number (GD07-W-2) when requesting detailed product information.
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