PEMF · full body mat
OMI Full Body PEMF Mat
An affordable low-intensity full-body mat that publishes a modest 2.2-gauss field with a clear 1 to 99 Hz range and a named sine waveform - a genuine spec, honestly small.
Flags
- · Markets FDA registration/listing, which is paperwork, not a 510(k) clearance.
By the numbers
- Format
- full body mat
- Field strength
- 220 µT at 1-99 Hz, published spec
- Frequency
- 1-99 Hz
- Waveform
- disclosed
- Adjustable
- frequency + intensity
- FDA status
- registered/listed only (not a clearance)
- Certification
- none published
- Applicators
- 1
- App / programs
- no
- Warranty
- 3 years
- Price
- $990
Strengths
- + Verified Field Spec: 8.0/10
- + Frequency & Programmability: 8.0/10
- + Value: 8.0/10
Watch-outs
- - Regulatory Honesty: 2.0/10
- - Markets FDA registration/listing, which is paperwork, not a 510(k) clearance.
Who it is for
- · Buyers who want a published field strength and frequency they can actually read off a spec sheet
- · People who want to set the frequency rather than run a single fixed program
- · Anyone who wants whole-body coverage in one session
Who should skip it
- · Buyers who read 'FDA registered' as a clearance - it is paperwork, not a clearance
How it scored
Verified Field Spec
8.0/10 · 30%A magnetic flux density in real units (microtesla or gauss) published WITH a stated frequency in Hz, ideally with the waveform. A unit-less intensity level or a peak with no frequency is not a usable spec.
- +6Published field strength at a stated frequency B220 µT at 1-99 Hz - A magnetic flux density in real units published together with a frequency, so the claim can be read and compared. The only field number we treat as usable.
- +2Waveform disclosed Bwaveform published - The pulse waveform is published, which is what an honest engineering spec looks like.
Regulatory Honesty
2.0/10 · 20%A real FDA 510(k) clearance (rare in consumer PEMF) versus FDA registration/listing used as if it were a clearance, plus electrical/EMC certification, recall history, and warranty.
- ·FDA registered/listed, not cleared Aregistration/listing only - FDA registration or listing is paperwork any maker can file; it is not a finding of effectiveness and not a 510(k) clearance.
- +2Long warranty B3-year - Three-year or longer warranty.
Frequency & Programmability
8.0/10 · 15%Whether frequency and intensity are adjustable across a stated range, and whether control is programmable.
- +4Adjustable frequency Bfrequency selectable - Lets you set the pulse frequency rather than a single fixed program.
- +3Adjustable intensity Bintensity selectable - Lets you set the field intensity.
- +1Stated frequency range B1-99 Hz - Publishes a frequency range rather than a single unstated value.
Coverage & Applicators
5.0/10 · 15%What the device actually covers: a full-body mat, a targeted local coil, or a wearable, and how many applicators it drives.
- +4Full-body mat coverage Bfull-body mat - A full-length mat covers the whole body in one session.
- +1Single applicator C1 applicator - One applicator.
Value
8.0/10 · 20%Price against the median for its format (full-body mat, targeted coil, or wearable).
- +8Price vs format median A$990 (bottom 20% of class (best value)) - Price scored against the median for its format. Format median about $5,890.
What to know before buying
- · Publishes a modest 2.2-gauss field at a clear 1 to 99 Hz range with a named sine waveform, which is a genuine spec rather than a peak headline.
- · FDA registered/listed as a wellness device, not 510(k) cleared; the sibling OMI Beyond mat steps up to about 10 gauss with extra waveforms.
- · Specs here are mirrored from an aggregator page; reconfirm against Oxford Medical Instruments before buying.
FAQ
- What field strength and frequency does the OMI mat actually publish?
- It states a modest 2.2-gauss field across a 1 to 99 Hz range with a named sine waveform. In our scoring that combination of a real unit and a stated frequency is a usable spec, so we credit it rather than capping it as a peak headline.
- Is the OMI mat FDA cleared?
- No. In our reading it is FDA registered/listed as a wellness device, which is paperwork rather than a 510(k) clearance, so we flag it on our regulatory axis and do not credit a clearance.
Last reviewed 2026-05-31. Scored under pemf-v1.0. See the methodology. Informational only, not medical advice. We score disclosure and specs, not health outcomes.