Category: Elekta ABSyndicate content

Elekta lands FDA win for next-generation linear accelerator

April 11, 2013 by Arezu Sarvestani

Elekta's next-generation Versa HD linear accelerator aims to provide faster and more efficient tumor targeting.

Elekta logo

Atlanta medical device company Elekta (STO:EKTA B) this week announced FDA clearance for its Versa HD linear accelerator, allowing the company to move forward with shipping and installations.

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McKesson to pay $2B for PSS World Medical | Wall Street Beat

October 25, 2012 by MassDevice staff

McKesson agrees to pony up more than $2 billion for medical supplies provider PSS World Medical.

MassDevice.com Wall Street Beat

McKesson (NYSE:MCK) agreed to pay $29 per share for PSS World Medical (NSDQ:PSSI) and its medical supplies business in a deal worth $2.1 billion.

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Japan approves Elekta's Agility radiation beam therapy system

July 31, 2012 by MassDevice staff

Global medical device company Elekta won Japanese regulatory approval for its Agility radiation therapy system, which boasts twice as many beam-shaping tungsten leaves as typical systems.

Elekta logo

Global medical device company Elekta (STO:EKTA B) won Japanese regulatory approval for its Agility radiation therapy system, which promises "faster, more accurate cancer treatments on the horizon."

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Bausch & Lomb wins FDA clearance for bio-inspired contact lenses | Regulatory Roundup

June 28, 2012 by MassDevice staff

Eye care giant Bausch & Lomb won FDA clearance for its Biotrue ONEday disposable contact lenses which contain the same water content as the cornea.

MassDevice.com Regulatory Roundup

 Bausch & Lomb touts FDA clearance for bio-inspired Biotrue contacts

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Biomet's prelims show improvement in U.S. ortho market | Wall Street Beat

June 19, 2012 by MassDevice staff

Analysts foresee a stable, and possibly improving, road ahead for the U.S. orthopedics market as bellwether Biomet releases preliminary Q2 earnings showing strong growth in knee and hip devices.

MassDevice.com Wall Street Beat

Things are looking up for the U.S. orthopedics market, as preliminary results for Biomet Inc.'s 2nd quarter suggest strong growth in domestic knee and hip devices sales.

Privately held Biomet, considered something of a bellwether for the U.S. orthopedics market, touted 6% year-over-year growth in knees and 8% in hips.

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Elekta shuffles the deck | Personnel Moves

June 5, 2012 by MassDevice staff

Swedish radiation therapy devices maker Elekta loses 2, adds 2 and promotes 1 within its leadership team.

fired/hired

 Elekta announces promotions, appointments and resignations

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FDA lets Cooper's Avaira Toric back on the market | Regulatory Roundup

April 6, 2012 by MassDevice staff

The FDA lets Cooper Cos. put its recalled Avaira Toric contact lenses back on the U.S. market; also, Delcath Chemsat component wins CE Mark; Elekta lands CE Mark for beam-shaper; new Steris product gets new device category, 510(k); Anulex touts expanded fiXate clearance; Fenwal wins 510(k) for plasma exchange protocol; Devon Medical's NPWT device wins FDA nod; Navidea wins Lymphoseek extension; and Estech gets conditional IDE for ATTAC-AF trial.

Avaira

Cooper Cos. (NYSE:COO) today announced that the U.S. Food and Drug Administration has granted a Special 510(k) clearance for CooperVision's Avaira Toric two-week silicone hydrogel contact lenses for astigmatism.

CooperVision will re-launch Avaira Toric with shipments available for select distribution beginning in early May 2012.

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