Friday, March 09, 2018 7:50:50 AM
2. What is the timeframe of the redesign of the acquired PEMF assets? When can we expect the human concussion clinicals to start?
3. CPAIR, Inc. Has finally moved forward with the manufacturing of their device. Does ENDV still have the license to sell Internationally? They stopped mentioning them in the financials but they may be due to the fact the CPAIR was stagnant for so long.
4. What is the next step with the heart device? Pre-clinicals are completed. Now what? Redesign for human heart testing? Plans for human clinicals?
Recent ENDV News
- Form SEC STAFF ACTION - SEC Staff Action: ORDER • Edgar (US Regulatory) • 09/19/2024 07:00:01 PM
- Form 15-12G - Securities registration termination [Section 12(g)] • Edgar (US Regulatory) • 02/02/2024 10:23:02 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 01/03/2024 10:30:14 PM
- Form 10-Q/A - Quarterly report [Sections 13 or 15(d)]: [Amend] • Edgar (US Regulatory) • 12/29/2023 08:20:36 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 12/04/2023 02:08:41 PM
- Form NT 10-Q - Notification of inability to timely file Form 10-Q or 10-QSB • Edgar (US Regulatory) • 11/15/2023 05:21:48 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/12/2023 10:03:32 AM
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