Donald R. Chase - 17 Aug 2026 Form 4 Insider Report for Bluejay Diagnostics, Inc. (BJDX)

Source evidence Original filing metadata and source links for verification. 4 source fields
SEC form
4
Accepted by SEC
18 Aug 2026, 16:15:24 UTC
Prior SEC filing
18 May 2026
Source filing
View source filing
Reporting owner 1 detail
Reporting owner signature
/s/ Donald R Chase

Key filing fact

Donald R. Chase filed Form 4 for Bluejay Diagnostics, Inc. (BJDX) on 18 Aug 2026.

Key facts

  • This page summarizes Donald R. Chase's Form 4 filing for Bluejay Diagnostics, Inc. (BJDX).
  • 1 reported transaction and 1 derivative row are listed below.
  • Accepted by SEC: 18 Aug 2026, 16:15.

Change

  • Previous filing in this sequence was filed on 18 May 2026.
  • Current net transaction value: $0.

Research use

  • This tells you what this filing adds before you inspect full transaction and derivative tables.
  • You can trace every row back to the original SEC filing document.

Evidence

Filed on Form 4

Ownership activity is grounded in SEC Form 4 disclosures.

View source filing

Reporting Owners (1)

CIK 0001247473 Primary reporting owner

CHASE DONALD R

Relationship
Director
Address
C/O BLUEJAY DIAGNOSTICS, INC., 360 MASSACHUSETTS AVENUE, SUITE 203, ACTON
Signature
/s/ Donald R Chase
Signature date
18 Aug 2026

Reported derivative securities

Options, warrants, convertible securities, or similar derivative positions disclosed in the filing.

BJDX transaction Derivative

Stock Option (Right to Buy)

Award

Transaction value
Shares
+100,000
Change %
Price
$0.000000*
Shares after
100,000
Date
17 Aug 2026
Ownership
Direct
Underlying class
Common Stock
Underlying amount
100,000
Exercise price
$2.08
Footnotes
F1
* marks a reported price that did not pass the local price check.

Additional SEC filing notes

Filing notes and footnotes

Explanation of responses 1 footnote

Footnote F1

Represents out-of-the-money stock options that vest and become exercisable for $2.075 per share on the first anniversary of the grant date, provided, however, that the options shall not be exercisable unless and until the U.S. Food and Drug Administration shall have granted clearance or approval of the issuer's Symphony IL-6 point-of-care testing device.

We use cookies and similar technologies to provide certain features, enhance the user experience and, if you allow them, measure engagement and deliver advertising. Analytics and marketing storage stay off until you grant consent. By clicking on "Agree and continue", you declare your consent to the use of the selected optional cookies. Manage preferences to update or revoke optional consent for future visits. For more information, see our Privacy Policy .