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Hooga HG1000

Hooga HG1000 product photo

Product image: Hooga product page.

The Hooga HG1000 is a lower-priced 35.8-inch panel with 200 LEDs using 660 nm red and 850 nm near-infrared light.

Hooga says it covers a standing adult from head to hip in one position; you reposition for the legs. A door mount and hanging kit are included, and Hooga offers a 3-year warranty and 60-day returns.

It's at the lower end on price for panels. It's narrower than the HG1500 and claims less power (98 mW/cm² at 6 inches), and we found no third-party measurement.

Lowest price we saw (price checked Nov 1, 2026)$599
No clearance found

Prices

StorePricePrice checked / source
Hooga (brand site)$599 Nov 1, 2026
brand store data		 View

Store links go straight to the store's product page, with no affiliate tracking. Confirm the price there before you buy. See our disclosure.

Price history

We don't have a sourced price history for this device yet. The prices above are what we saw on the dates shown. A current sale price isn't necessarily the lowest this device has sold for.

Specs & regulatory status

Size (height)35.8 in (91 cm)
Panel only: 35.8″ × 8.2″. Brand spec. source
Wavelengths660 nm, 850 nm source
Power claimed (irradiance)98 mW/cm²
At 6 in (brand).
source
Power measured (available third-party measurement)No third-party measurement found yet.
FDA statusNo clearance found
Registration/listing with FDA is not the same as a 510(k) clearance. No 510(k) found in FDA's database by brand or product name.

"No clearance found" means we found no matching record in the FDA's database. That doesn't prove no clearance exists. FDA clearance is not FDA approval, and a listed specification isn't proof that a device works. How we check FDA status.

Terms on this page

nm
Nanometres, the unit for a light's wavelength (its colour). Red light is roughly 620–700 nm; near-infrared is above 700 nm.
mW/cm²
Milliwatts per square centimetre: how much light power reaches each square centimetre of skin (irradiance).
510(k)
The FDA premarket notification route. A cleared 510(k) means the FDA found the device substantially equivalent to one already on the market. It is not FDA approval.