Bobby, the FDA updated the Well-Life Registration this week
The update shows that Well-Life is a contract mfg for Hi-Dow not BIEL. When Hi-Dow got their Prescription Only Clearance in 2020 they had an elaborate PEMF offering at around $1k. That product is no longer on their website, they must have something new in the works.
With CICD no longer on the FDA Registration site and Well-Life confirmed as working for Hi-Dow, this adds weight to the Licensing theory. If Electrome is producing their own PEMF device, Licensed from BIEL, they would still need to get their mfg registered with the FDA.
Lots of variables at play:
* If BIEL has been working with Electrome all year CICD would have had time to do a production run while still FDA Registered
* If Electrome wants a quick entry to market with a standard ActiPatch or RecoveryRx BIEL may have enough devices in inventory
* If Electrome wanted to use a US mfg to avoid the ever changing tariffs they could have Viant do the mfg. registering in 2026
* etcetera
IMO, minus Well-Life, there is still extensive evidence that BIEL and Electrome are working together.
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