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Home » Authors » Stacy Lawrence

Articles by Stacy Lawrence

Insulet achieves 2018 profitability, preps for hybrid closed-loop, interoperability

Feb. 27, 2019
By Stacy Lawrence

Wall Street embraces GE sale of Biopharma biz to Danaher for $21.4B, puts IPO in doubt

Feb. 26, 2019
By Stacy Lawrence
General Electric Co.'s (GE) spinout of its Healthcare business in an IPO has been a highly anticipated med-tech industry event for 2019. But now all that is back into play. The Boston-based conglomerate has opted to sell its Biopharma business for $21.4 billion to Danaher Corp. That Biopharma unit accounted for about 15 percent, or about $3 billion, of the almost $20 billion in 2018 Healthcare revenues.
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Wall Street embraces GE sale of Biopharma biz to Danaher for $21.4B, puts IPO in doubt

Feb. 26, 2019
By Stacy Lawrence
General Electric Co.'s (GE) spinout of its Healthcare business in an IPO has been a highly anticipated med-tech industry event for 2019. But now all that is back into play. The Boston-based conglomerate has opted to sell its Biopharma business for $21.4 billion to Danaher Corp. That Biopharma unit accounted for about 15 percent, or about $3 billion, of the almost $20 billion in 2018 Healthcare revenues.
Read More

Specter of US pricing pressure weighs on Dexcom as CGM competition intensifies

Feb. 25, 2019
By Stacy Lawrence
In the last year, Dexcom Inc., of San Diego, has seen its market cap grow exponentially – from less than $5 billion in February 2018 to roughly $12.5 billion now. That followed about three years of stagnant valuation for the continuous glucose monitor (CGM) player. The strength of the recent Dexcom run-up has been on the thesis of widespread U.S. market penetration, particularly as it became the first CGM player to gain Medicare reimbursement.
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Chinese researchers test feasibility of self-powered pacemaker in a pig model

Feb. 21, 2019
By Stacy Lawrence

FDA establishes new interoperable insulin pump device class – with Tandem up first

Feb. 19, 2019
By Stacy Lawrence
Tandem Diabetes Care Inc. saw its shares climb almost 20 percent this week, just as it became the first company to have a product classified in a new FDA category: Alternate Controller Enabled Infusion Pumps (ACE pumps).
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Ophthalmic drug-device maker Avedro prices $70M IPO, but at bottom of offering range

Feb. 15, 2019
By Stacy Lawrence
Avedro Inc. squeaked out the door with its IPO. It managed to raise $70 million, rather than the $75 million it had previously proposed, after pricing at the bottom of its $14 to $16 per share range. The ophthalmic med-tech company held the number of shares steady at the proposed 5 million. Still, shares (NASDAQ:AVDR) slipped by about 12 percent to $12.25 in early trading.
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J&J to buy its robotic endoscopy partner Auris Health in deal worth up to $5.75B

Feb. 14, 2019
By Stacy Lawrence

The rumors of an acquisition of Auris Health Inc. by New Brunswick, N.J.-based Johnson & Johnson (J&J) have been around for a few weeks, since right around the latter's annual earnings report on Jan. 22. Now the conglomerate has confirmed that its Ethicon Inc. subsidiary will acquire Redwood City, Calif.-based Auris for $3.4 billion in cash and up to an additional $2.35 billion in undisclosed milestones.


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Edwards to buy partner Casmed for $100M to add noninvasive brain oxygenation monitor

Feb. 13, 2019
By Stacy Lawrence
Edwards Lifesciences Corp. will acquire micro-cap Cas Medical Systems Inc. (Casmed) for about $100 million. The pair were partnered already on 510(k) clearance-pending cable and software to connect Casmed's Fore-Sight brain tissue oxygenation monitor to Edwards' Hemosphere hemodynamic monitoring platform for surgery and critical care.
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Biodirection granted breakthrough designation for Tbit portable traumatic brain injury test

Feb. 12, 2019
By Stacy Lawrence
Biodirection Inc. has won Breakthrough Device Designation from the U.S. FDA for its Tbit system for the prediction of positive computerized tomography (CT) scans following traumatic brain injury (TBI). The Boston, Mass.-based company expects to shepherd an emergency room-oriented diagnostic through the 510(k) de novo process and onto the market potentially by the end of the first quarter of 2020.
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