Search For "fda"
Nesa Medtech receives US FDA clearance for its fibroid mapping reviewer ap
Updated : 2 years, 8 months ago IST
Bengaluru (Karnataka) [India], July 24: Nesa Medtech (Nesa), a private medical device company addressing clinical unmet needs for patients with symptomatic uterine fibroids, announced today that it received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the company's F
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US, India conduct 'Operation Broader Sword' to stop international shipment
Updated : 2 years, 8 months ago IST
Conducted in June 2023, Operation Broader Sword stopped more than 500 shipments of illicit, and potentially dangerous, unapproved prescription drugs, combination medical devices, and synthetic drug precursors from reaching American consumers, the US Embassy in India said in a press release.
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Maharashtra Speaker Rahul Narvekar asks DGP to ensure cows are not slaught
Updated : 2 years, 8 months ago IST
"It was brought to our notice by some organizations that cow protectors are being attacked in many places and the law is being ignored even though there is a law on cow slaughter," he told ANI.
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La Pink introduces 100 per cent Microplastic Free Formulations in skincare
Updated : 2 years, 9 months ago IST
New Delhi [India], June 2: Revolutionising the beauty and skincare market in India, La Pink has introduced innovative 100 per cent microplastic-free skincare formulations for the first time in the country. La Pink's ground-breaking products have been created by French experts after months of
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BrowMaster Now Offering Scalp Micro Pigmentation (SMP) Services in India
Updated : 2 years, 9 months ago IST
New Delhi [India], June 2: Scalp micropigmentation (SMP) is a non-surgical cosmetic procedure that uses a tattooing technique to create the appearance of fuller hair. It can be a good option for people who are self-conscious about their hair loss or scalp showing through. Scalp Micropigmenta
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Concept Medical's fourth IDE approval for the MagicTouch Sirolimus Coated
Updated : 2 years, 9 months ago IST
Tampa (Florida) [US], May 29: The US FDA, on the 24th of May 2023, granted an Investigational Device Exemption (IDE) approval for Concept Medical Inc's Sirolimus Coated Balloon (SCB) MagicTouch PTA for the treatment of Superficial Femoral Arteries (SFA). This marks the fourth IDE approval
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Musk brain-chip firm Neuralink gets US regulator nod to conduct its first
Updated : 2 years, 10 months ago IST
In a tweet, Neuralink expressed its excitement, "We are excited to share that we have received the FDA's approval to launch our first-in-human clinical study! This is the result of incredible work by the Neuralink team in close collaboration with the FDA and represents an important first
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Wellthy Therapeutics announces expansion into the United States - complete
Updated : 2 years, 10 months ago IST
Mumbai (Maharashtra) [India]/ Los Angeles (California) [US], May 11 (ANI/PRNewswire): Wellthy Therapeutics, a global leader in digital health and digital therapeutics, announces the successful completion of its FDA 21 CFR Part 820, FDA 21 CFR Part 11, and HIPAA certification for its diseas
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US Food and Drug Administration recalls some COVID-19 at-home tests over b
Updated : 2 years, 10 months ago IST
The US FDA stated that the decision was taken over "significant concerns" of bacterial contamination.
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MedAlliance enrolls first US patient into its third FDA IDE Study: SFA SEL
Updated : 2 years, 10 months ago IST
Geneva [Switzerland], May 5 (ANI/PRNewswire): The first US patient has been enrolled in the SELUTION4SFA Sirolimus DEB study by Dr Arthur Lee at the Cardiac & Vascular Institute in Florida. This study evaluates SELUTION SLR™ in the treatment of occlusive disease of the superficial
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Concept Medical received IDE approval to investigate safety and efficacy o
Updated : 2 years, 10 months ago IST
Tampa (Florida) [US], May 1 (ANI/PRNewswire): The US FDA has granted an Investigational Device Exemption (IDE) approval for Concept Medical Inc's novel MagicTouch Sirolimus Coated Balloon (SCB) for the treatment of Small Vessels (SV) in coronary arteries.
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"Someone duplicated cough syrup to defame India": Managing Director, QP Ph
Updated : 2 years, 11 months ago IST
"Food And Drug Administration (FDA) of Punjab doubt that someone has duplicated the product (cough syrup) sent to Cambodia and then sold it in the Marshall Islands and Micronesia to defame the Government of India," said Sudhir Pathak, MD of the firm based in Dera Bassi, Punjab .
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