TexasMarvL
2 days ago
Another detail I wanted to share from the 10K.
PAGE 14.
"On February 20, 2024, AXIM announced that Verséa™ Ophthalmics, LLC, placed an order for an additional 50 of IUL Lateral Flow Readers."
ONLY 50 READERS????
I realize $2000 per reader adds up quickly.
50 × $2000 = $100,000.
BUT
If AXIM and Verséa were anywhere close to CLIA Waiver approval, they would not order just 50 readers. If CLIA Waiver is anywhere close to approval there would be an order of 300 or 500 or 1000 readers.
Besides that, according to one post or video some customers are purchasing two readers so they can run both tests concurrently to save time.
Look at AXIM realistically.
This company has a lot of potential and hopefully just a few months down the road.
Keep watching.
Hang on to some dry powder.
About the only things to budge AXIM share price in the short-term is a potential merger or acquisition or a new merchandising agreement for the Parkinsons disease test. I do think AXIM has to consider a merchandising agreement for the Parkinsons disease test because they are bleeding too much cash right now.
TexasMarvL
3 days ago
Auer Precision was mentioned exactly 1 time.
The Parkinson Disease test was mentioned exactly one time.
Page 30
========
Revenues. $ 39,518
Net loss. $(8,059,682)
Page F4
========
Common stock, $0.0001 par value, 1,000,000,000 shares authorized 245,929,403 and 192,441,917 shares issued and outstanding, respectively.
Page F28
˜========
The Company has authorized 1,000,000,000 shares of common stock, with a par value of $0.0001 per share. As of December 31, 2023, and 2022, the Company had 245,929,403 and 192,441,917 shares of common stock issued and outstanding, respectively.
2023 Transactions:
The Company converted debt of $380,858 including accrued interest of $30,858 in exchange for 22,207,486 shares.
these shares were issued at $0.031 resulting in extinguishment of debt Beneficial conversion payment of interest ($688,432) and Debt modifications / conversions feature worth ($459,522).
Common stock issued under s-1 23,000,000 shares in exchange for cash $514,931.
Common Stock issued stock purchase agreement 7,280,000 in exchange for equipment valued at $72,800 and recorded a loss on issuance of $80,080.
TexasMarvL
3 days ago
Just for grins I cut/pasted the CLIA forward looking statement paragraph from 2023 and 2024. At least John remembered to change the year.
Bottom line. Verséa will have to help with the CLIA Waiver or it will not get done.
AXIM Biotechnologies, Inc. - 10K - Annual Report - April 17, 2023
The FDA allows for a CLIA waiver, and we intend to pursue a waiver for both current tests and all future product offerings. Our scientists have been diligently making patentable improvements to the tests which will simplify use by the clinician and enhance likelihood the CLIA waiver approval. We plan to file for the waiver early in the second quarter of 2023 after conducting a fairly simple comparative clinical study. The objective will be to determine whether the AXIM Eye test system has equal or better simplicity than the other forms of diagnostic testing for DED, which we believe is the case. This study is a key component of the filing process with the FDA for a Clinical Laboratory Improvement Amendment (CLIA) Certificate of Waiver. We believe that the acquisition of these FDA 510k cleared diagnostic products, a waiver and the distribution partnership we have with Versea will allow the business to grow at a rapid pace.
AXIM BIOTECHNOLOGIES, INC.
FORM 10-K
FOR THE YEAR ENDED DECEMBER 31, 2023
TABLE OF CONTENTS
The FDA allows for a CLIA waivers, and we intend to pursue a waiver for both current tests and all future product offerings. Our scientists have been diligently making patentable improvements to the tests which will simplify use by the clinician and enhance likelihood of CLIA waiver approval. We plan to file for the waiver in the second quarter of 2024 after conducting a fairly simple comparative clinical study. The objective will be to determine whether the AXIM Eye test system has equal or better simplicity than the other forms of diagnostic testing for DED, which we believe is the case. This study is a key component of the filing process with the FDA for a Clinical Laboratory Improvement Amendment (CLIA) Certificate of Waiver. We believe that the acquisition of these FDA 510(k) cleared diagnostic products, a waiver and the distribution partnership we have with Versea will allow the business to grow at a rapid pace.
mc73
4 days ago
You might want to start thinking of taking your losses and moving on. If not now, when? Another year? 2 years? There has to be a point where you realize nothing will happen here. It might not be to that point yet, but it seems to be getting close imo. I'll watch this for another year and if it is more of the same, I won't even follow on here and iHub any longer.
Hopefully, in the next year, this company produces some results.