US-based HD Medical has announced the launch of its ViScope MD visual stethoscope with murmur detection indicator at MEDICA, 20 November through 23 November 2013, in Germany. ViScope MD features an integrated visual display which allows ...
Tags: HD Medical, Medicine
CIVCO Medical Solutions, a medical technology company, has obtained 510(k) clearance from the US Food and Drug Administration (FDA) for its EX3 stepper, which is used while performing real time planning for low dose rate (LDR) or high dose ...
Tags: CIVCO Medical, Medicine
TauTona, a medical device firm, has obtained 510(k) approval from the US Food and Drug Administration (FDA) and a new patent from the US Patent and Trademark Office (USPTO) for the TauTona tissue injector (TTI), a hand-held adipose tissue ...
Tags: Tautona, Transfer Tool
Medtronic's Valiant 'Mona LSA' branch thoracic stent graft system demonstrated proof of concept in a first-in-human study being conducted under the US Food and Drug Administration (FDA)'s ‘Innovation Pathway’ early feasibility ...
Tags: stent graft system, Medicine
US-based Illumina has obtained premarket clearance from the US Food and Drug Administration (FDA) for the MiSeqDx system, a high-throughput DNA sequencing analyzer. The company has also obtained premarket clearance from the FDA for the ...
Tags: Illumina, MiSeqDx System
Boston Scientific, a medical device company, has obtained the US Food and Drug Administration clearance and CE Mark approval for its Direxion torqueable microcatheter, designed to facilitate selective access and delivery of diagnostic, ...
Tags: Boston Scientific, Microcatheter
The US Food and Drug Administration (FDA) has accepted AstraZeneca's new drug application (NDA) for naloxegol, an investigational peripherally-acting mu-opioid receptor antagonist (PAMORA). The drug has been studied in opioid-induced ...
Tags: Drug Application, FDA Approval
Intellipharmaceutics International has announced that the US Food and Drug Administration (FDA) has granted final approval of the company's dexmethylphenidate hydrochloride extended-release capsules for the 15 and 30mg strengths. ...
Tags: Focalin XR, Medicine
Valeant Pharmaceuticals North America, a wholly-owned subsidiary of Valeant Pharmaceuticals International, has received a notice that the new drug application for Luzu (luliconazole) cream, 1% has been approved by the US Food and Drug ...
NEC Display Solutions of America, a provider of commercial LCD display and projector solutions, has obtained 510(k) clearance from the US Food and Drug Administration (FDA) for its MultiSync MD210C2 medical-grade monitor. The 21.3-inch, ...
Tags: NEC Display Solutions, Medicine
Merck has secured priority review status from the US Food and Drug Administration (FDA) for its new drug application (NDA) for an investigational intravenous (IV) solution formulation of its antifungal agent, Noxafil (posaconazole), ...
The US Food and Drug Administration (FDA) has classified Medtronic's recently initiated voluntary field action related to certain guidewires as a class I recall. The company initiated recalling some models of its guidewires from recent ...
Tags: Certain Guidewires, Medtronic
Lumenis has obtained the US Food and Drug Administration (FDA) and the Japanese Ministry of Health, Labour and Welfare (MHLW) approvals for its Array LaserLink pattern scanning device for multi-spot laser photocoagulation for use during ...
Tags: Lumenis, Laser Treatment
Garden-Fresh Foods, a US-based food firm, has halted operations at its production facility in Milwaukee over product recalls. The company has recalled tons of products in five recalls since August-end, as Michigan state food safety ...
Tags: Product Recalls, Garden-Fresh
US-based Escalon Medical has announced its plans to introduce a new tablet-based ultrasound imaging system, the Sonomed Escalon VuPad, at the upcoming 117th Annual Meeting of the American Academy of Ophthalmology (AAO), 16 November to 19 ...