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Navient receives FDA 510(k) clearance for ENT procedures
CKI (ClaroNav Kolahi Inc.) has received FDA 510(k) clearance for Navient in ENT procedures, expanding its previous clearance for cranial applications. Navient is now approved by major global regulatory bodies, including Canada (HC), Europe (EU MDD), China (NMPA), UAE, Saudi...Soluvos Medical is looking forward to catching up with readers
Having recharged their batteries and the Soluvos Medical team is looking forward to meeting readers again at the next symposia and hands-on courses. Pass by their booth to catch up and to meet their new Sales Manager - Marc de...Neuromod advances multiple regulatory approvals to expedite Lenire’s global availability
Neuromod, the medical technology company that created the Lenire® tinnitus treatment device, has announced approval to the Medical Device Single Audit Program (MDSAP) and EU Medical Device Regulation (MDR) certification. Neuromod’s MDSAP certification follows a comprehensive audit verifying compliance with...From Irish innovation to Global impact: Tympany Medical seeks investors
Irish MedTech pioneer Tympany Medical has launched a €600,000 crowdfunding campaign via Crowdcube under the Employment and Investment Incentive Scheme (EIIS), offering a 50% tax rebate for Irish taxpayers. The campaign invites both seasoned and first-time investors to back innovation...
