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of The VisAbility micro insert

1, VISABILITY™ MICRO INSERT SYSTEM FDA 网页The VisAbility Micro Insert System has been in development over the last 20 years as a treatment for presbyopia. The VisAbility Micro Insert ystem is uni...
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1, VISABILITY™ MICRO INSERT SYSTEM FDA

网页The VisAbility Micro Insert System has been in development over the last 20 years as a treatment for presbyopia. The VisAbility Micro Insert ystem is unique among S ocular

Scleral Inserts | Ento Key

网页2019年9月1日 · These theories provide the basis for a scleral solution to restore dynamic accommodation. The VisAbility Micro-Insert System (Refocus Group) is a binocular presbyopia correction procedure performed outside the visual axis. Unlike static corrections such as corneal inlay technologies, monovision or multifocal laser vision correction, and

History of Changes for Study: NCT02374671

网页A Clinical Trial of The VisAbility Micro Insert System for Presbyopic Patients Latest version (submitted December 17, 2019) on ClinicalTrials.gov A study version is represented by a row in the table.

Scleral Surgery for Presbyopia | Ento Key

网页2019年10月10日 · In a 24-month clinical trial with VisAbility Micro-Insert trials presented in 2013, 80 patients were asked to describe their unaided vision as “excellent,” “acceptable,” or “poor,” pre- and postoperatively. At 24 months, 73% patients

Clinical Trial on Presbyopia: VisAbility Micro Insert - Clinical

网页The purpose of this study is to evaluate the safety and effectiveness of the VisAbility Micro Insert System for the improvement of near visual acuity in .. Sponsors Lead Sponsor: Refocus Group, Inc. Source Refocus Group, Inc. Brief

Sclera Based Solutions to Presbyopia and the Aging Lens

网页Figure 1. Implantation of the VisAbility Micro Insert. Figure 2. The LSM procedure performed with the VisioLite device. Reprinted with permission from Hipsley et al.11 Figure 3. The LSM procedure performed with the VisioLite Gen I

VisAbility Micro Insert System

网页VisAbility Micro Insert System Instructions for Use Refocus Group, Inc. 92028 IFU v1 / ADYTPM Page 3 of 16 2. Peritomy Re-instill sterile 2% xylocaine drops without

Sclera-Based Solutions to Presbyopia and the Aging Lens

网页Implantation of the VisAbility Micro Insert. In January, results of a 360-patient FDA clinical trial with the device were posted on clinicaltrials.gov. 5 In this trial, patients at 14 sites received VisAbility Micro Inserts in their first eye, then

MillennialEYE | VisAbility Micro-Insert System for Presbyopia

June 9, 2020: Ophthalmic Devices Panel meeting

网页2020年4月28日 · The VisAbility Micro Insert is indicated for bilateral scleral implantation to improve unaided near vision in phakic, presbyopic patients between the ages of 45 and 60 years of age, who have a

History of Changes for Study: NCT03811249

网页Long Term Follow-up of the VisAbility Micro Insert System for Presbyopic Patients Latest version (submitted October 15, 2019) on ClinicalTrials.gov A study version is represented by a row in the table.

Capwell Communications | Public Relations

网页Strategic positioning, corporate and product PR for the VisAbility Micro insert for the treatment of presbyopia. Refractec Strategic positioning and award-winning publicity campaign for conductive keratoplasty (CK) turned this

Brief Summary Ophthalmic Devices Panel of the Medical

网页The VisAbility Micro Insert is indicated for bilateral scleral implantation to improve unaided near vision in phakic, presbyopic patients between the ages of 45 and 60 years of age, who have a

The future of refractive surgery: presbyopia treatment, can we

网页2020年9月7日 · Currently, the VisAbility Micro-Insert scleral implant (Refocus Group, Dallas, TX, USA) has a CE mark and is currently undergoing clinical trials []. However, there are risks from anterior segment

Going Small with Big Results: The VisAbility Micro-Insert System

网页2017年6月1日 · The VisAbility Micro-Insert from Refocus Group is the first and only presbyopic procedure performed outside the visual axis. by Michael Smolinsky, PhD, Chief Content Officer, Ethis In May of this year, Refocus Group (Dallas, TX) announced that it had completed enrollment of its Phase 3 clinical trial on the VisAbility™ Micro-Insert System

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