This briefing describes the regulated use of the technology for the indication specified, in the setting described, and with any other specific equipment referred to. It is the responsibility of ...
Icare ic200, the new generation tonometer for intraocular pressure screening for professional use has been cleared by FDA, the Food and Drug Administration of the United States. The product has been ...
Recently, a new rebound tonometer has been introduced into the market, which might be useful for glaucoma screenings in developing countries. Disposable probes, that are potentially reusable, are ...
Please provide your email address to receive an email when new articles are posted on . In three consecutive studies, rebound tonometry with iCare technology showed greater precision than standard ...
To compare intraocular pressure (IOP) measurements with Goldmann applanation tonometry (GAT) and iCare tonometry in normal and post-keratoplasty corneas and to assess the influence of central corneal ...
Revenio Group Oyj, provides ophthalmological devices and software solutions for the diagnosis of glaucoma, macular degeneration, and diabetic retinopathy in Finland, the United States, and ...
Please provide your email address to receive an email when new articles are posted on . The iCare Home2 yielded similar results as the Goldmann applanation tonometer. Researchers recommend central ...
Revenio Group`s subsidiary, Icare Finland Oy has received a marketing approval for the Icare HOME tonometer in the United States. In late November 2016, the company filed a supplemented Premarket ...
Real Potential for Self-tonometry? Glaucoma is often a disease of subtleties. A tiny notch of rim tissue, an extra point of visual field depression, or even a single 1-mm Hg change in intraocular ...
HELSINKI, March 16, 2021 /PRNewswire/ -- Icare Finland, a trusted partner in providing fast, easy-to-use, and reliable tools for ophthalmic diagnostics, is launching their next generation ...
A search of the Medicines and Healthcare Products Regulatory Agency website revealed no manufacturer Field Safety Notices or Medical Device Alerts for this device. There were 2 reports representing 1 ...
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