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Orion Portfolio Solutions LLC Lowers Stock Position in Hologic, Inc. (NASDAQ:HOLX) - Vimarsana News

Orion Portfolio Solutions LLC Lowers Stock Position in Hologic, Inc. (NASDAQ:HOLX)

Orion Portfolio Solutions LLC decreased its holdings in Hologic, Inc. (NASDAQ:HOLX – Free Report) by 14.5% in the 4th quarter, according to the company in its most recent 13F filing with the Securities and Exchange Commission (SEC). The fund owned 63,622 shares of the medical equipment provider’s stock after selling 10,800 shares during the quarter. […]

DelveInsight Business Research, LLP: Global Immunoassay Market to Witness Growth at a CAGR of ~8% by 2030 - Vimarsana News

DelveInsight Business Research, LLP: Global Immunoassay Market to Witness Growth at a CAGR of ~8% by 2030

The surge in the immunoassay market is mainly from the rising occurrence of persistent conditions like cancer and lifestyle-related ailments such as diabetes mellitus. Notably, the uptick in

Founders can follow different strategies to success - Vimarsana News

Founders can follow different strategies to success

If there’s a common trait among effective entrepreneurs, it’s their tendency to follow unique paths to success.

Congress Wealth Management LLC DE Sells 22,076 Shares of Hologic, Inc. (NASDAQ:HOLX) - Vimarsana News

Congress Wealth Management LLC DE Sells 22,076 Shares of Hologic, Inc. (NASDAQ:HOLX)

Congress Wealth Management LLC DE reduced its holdings in shares of Hologic, Inc. (NASDAQ:HOLX – Free Report) by 17.2% in the 4th quarter, according to its most recent filing with the Securities & Exchange Commission. The institutional investor owned 105,917 shares of the medical equipment provider’s stock after selling 22,076 shares during the quarter. Congress […]

Hologic, Inc. Recalls BioZorb Marker Due to Complications with Implanted Devices - Vimarsana News

Hologic, Inc. Recalls BioZorb Marker Due to Complications with Implanted Devices

The U.S. Food and Drug Administration (FDA) has issued a recall of the Hologic, Inc. BioZorb marker due to complications with implanted devices. The agency identified this as a Class I recall, the most serious type of recall. Details issued in a written notice by the FDA on May 22 and are shared here.