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491,520 Results for "remedent inc".
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Genetown
ZOLL remedē System, a Breakthrough Therapy for Treating Central Sleep Apnea, Receives Approval for MRI Conditional Use
ZOLL® Medical Corporation, an Asahi Kasei company that manufactures medical devices and related software solutions, announced today that the United States Food and Drug Administration (FDA) has approved the remedē System for conditional use with magnetic resonance imaging (MRI).
May 24, 2023
·
7 min read
Press Releases
Stonegate Updates Coverage on Incannex Healthcare Inc. (IXHL) FY26
October 1, 2026
·
2 min read
Policy
Remedent, Inc. Files Form 15 to Suspend SEC Exchange Act Registration and Applies to Qualify for OTC Markets Alternative Reporting Standard for Pink Sheet Companies
Remedent, Inc. announced the voluntary filing of a Form 15 with the United States Securities and Exchange Commission to terminate the registration of its common stock under Section 12 Securities Exchange Act of 1934, as amended and suspend its SEC reporting obligations under Section 15 of the Exchange Act.
June 30, 2021
·
3 min read
BioMidwest
Respicardia Announces Highmark Coverage for the remedē® System in Patients with Central Sleep Apnea
Respicardia, Inc., the manufacturer of the only FDA-approved active implantable system for the treatment of central sleep apnea, announced that Highmark Blue Cross Blue Shield and its affiliates will provide coverage for the Company’s remedē® System therapy, effective immediately.
January 7, 2021
·
4 min read
Remedent announces its agreement with Aurum Ceramic Dental Laboratories Co., concerning an Exclusive Master License Agreement in reference to its GlamSmile Veneers and Technology
Remedent, Inc., an international company specializing in research, development, and manufacturing of oral care and cosmetic dentistry products, announces its agreement to provide GlamSmile veneers and Technologies to Aurum Ceramic Dental Laboratories Co., for the territory of North America.
June 1, 2021
·
4 min read
FDA
ZOLL Announces Approval of Next-Generation remedē System for the Treatment of Central Sleep Apnea (Transvenous Phrenic Nerve Stimulation)
ZOLL® Medical Corporation, an Asahi Kasei company that manufactures medical devices and related software solutions, announced today that it has received U.S. Food and Drug Administration (FDA) approval for the remedē® EL-X System to treat moderate to severe Central Sleep Apnea (CSA) in adult patients.
August 5, 2021
·
7 min read
Press Releases
Mint Pharmaceuticals Inc. and Bayer Inc. Expand Distribution Partnership in Canada
October 6, 2026
·
3 min read
Genetown
ZOLL Announces Five-Year Study Confirming Safety, Efficacy and Beneficial Effects of Long-Term Transvenous Phrenic Nerve Stimulation (the remedē System)
ZOLL® Medical Corporation, an Asahi Kasei company that manufactures medical devices and related software solutions, announced today that the peer-reviewed journal Nature and Science of Sleep has published five-year results from the remedē System Post Approval Study
May 17, 2021
·
8 min read
BioMidwest
Transvenous phrenic nerve stimulation (The remedē System) shows sustained safety and efficacy through 5 years
Respicardia has announced 5-year results from the remedē System Post Approval Study, assessing the safety and efficacy of transvenous phrenic nerve stimulation for the treatment of moderate to severe central sleep apnea (CSA).
October 20, 2020
·
5 min read
Press Releases
RxSight, Inc. Reports Third Quarter 2026 Results
November 3, 2026
·
11 min read
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