BlissGlows LaserRevive™ 352 | FDA Cleared Laser Hair Growth Helmet
BlissGlows LaserRevive™ 352 | FDA Cleared Laser Hair Growth Helmet
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Advanced 352-Laser Technology for At-Home Hair Growth
Meet the BlissGlows ReviveX™ 352, an advanced Low-Level Laser Therapy (LLLT) helmet designed to deliver convenient, hands-free laser treatment across the scalp from the comfort of home.
Featuring 352 laser diodes operating at 650nm, ReviveX™ 352 combines extensive scalp coverage with a simple treatment routine for men and women experiencing qualifying androgenic alopecia.
352 Precision Laser Diodes
ReviveX™ 352 uses 352 low-level laser diodes positioned throughout the helmet to provide broad exposure across the scalp.
The FDA 510(k) documentation specifies a 650nm laser wavelength and laser diode energy of less than 5mW per diode.
FDA 510(k) Cleared
The Laser Helmet 352 is FDA 510(k) cleared under K253231 and classified as a Class II medical device under product code OAP.
The FDA-cleared indication is to promote hair growth in males with androgenic alopecia who have Norwood-Hamilton classifications IIa–V and females with androgenic alopecia who have Ludwig-Savin classifications I–II, with Skin Phototypes I–IV.
See the ReviveX™ 352 in Action
Discover how the 352-laser hair growth helmet fits into a simple, hands-free at-home treatment routine.
Why You'll Love It
- 352 Laser Diodes: Designed to provide extensive laser coverage across the scalp.
- 650nm Laser Technology: Uses Low-Level Laser Therapy technology at a 650nm wavelength.
- FDA 510(k) Cleared: Laser Helmet 352 is cleared under K253231.
- Hands-Free Treatment: Helmet-style design makes it convenient to use during your regular routine.
- 30-Minute Sessions: Designed for a straightforward treatment schedule.
- For Men & Women: FDA-cleared indications include qualifying male and female androgenic alopecia.
How Low-Level Laser Therapy Works
ReviveX™ 352 is a dome-shaped Low-Level Laser Therapy (LLLT) device designed to expose the scalp to laser light therapy as part of its FDA-cleared hair-growth indication.
Simple 30-Minute Treatment Routine
According to the FDA 510(k) documentation, the Laser Helmet 352 has a maximum treatment time of 30 minutes and a treatment frequency of 3 times per week, spaced every other day.
- Monday — 30 minutes
- Wednesday — 30 minutes
- Friday — 30 minutes
Always follow the user manual and instructions supplied with your device.
Who Is ReviveX™ 352 Designed For?
According to the FDA-cleared indications for use, the Laser Hair Growth System is indicated to promote hair growth in:
- Males with androgenic alopecia classified as Norwood-Hamilton IIa–V.
- Females with androgenic alopecia classified as Ludwig-Savin I–II.
- Individuals within Skin Phototypes I–IV.
Technical Specifications
| Model | Laser Helmet 352 |
| Technology | Low-Level Laser Therapy (LLLT) |
| Laser Diodes | 352 |
| Laser Wavelength | 650nm |
| Energy Per Laser Diode | <5mW |
| Energy Density | 2.74 mW/cm² |
| Laser Classification | Class 3R |
| Maximum Treatment Time | 30 minutes |
| Treatment Frequency | 3 times per week, every other day |
| FDA 510(k) | K253231 |
| FDA Classification | Class II |
| Product Code | OAP |
Advanced Hair-Growth Technology at Home
BlissGlows ReviveX™ 352 combines high-density laser coverage with a hands-free helmet design, making Low-Level Laser Therapy easier to incorporate into a consistent at-home hair-growth routine.
Important Information
Results may vary between individuals. Use the device only according to the supplied instructions and user manual.
Consult an appropriate healthcare professional if you have questions about hair loss, an underlying medical condition, or whether this device is appropriate for you.
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