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Jul 20, 2026, 08:47 ET Robert Lewandowski v novej televíznej reklame značky CHERY - oživenie kampane „Pre rodinu"
vlastnostiach vozidla, ale aj o emocionálnej hodnote, ktorá sa skrýva za rodinnou mobilitou."Pre rodinu" nie je pre značku CHERY len sloganom. Ide o dlhodobý záväzok, ktorý usmerňuje vývoj produktov, technologické inovácie a budovanie globálnej značky. Priestor. Pre rodinu. Bezpečnosť. Pre rodinu.
More news about: Chery Automobile Co., Ltd.
Jul 17, 2026, 11:17 ET Bamboo Expands Greenshoots Re Sidecar with Fourth Fronting Carrier, Growing Facility to Approximately $175 Million
fronting carriersMIDVALE, Utah, July 17, 2026 /PRNewswire/ -- Bamboo Ide8 Insurance Services, LLC ("Bamboo") announced the completion of a multi-year sidecar transaction through Greenshoots Re Ltd. ("Greenshoots Re") supporting
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Jul 17, 2026, 09:00 ET IDEAYA Biosciences Announces ESMO 2026 Presentations for Darovasertib and IDE849 Clinical Programs
development programs, including the potential therapeutic benefits, clinical profile, and differentiating characteristics of darovasertib, IDE849, IDE892 and IDE397; the timing conduct and anticipated results of ongoing and planned clinical trials, including anticipated initiation of registrational trials;
More news about: IDEAYA Biosciences, Inc.
Jul 16, 2026, 10:24 ET Technologický pokrok, ktorý stojí za platformou novej generácie pre inteligentný stringový systém na vytváranie sietí na skladovanie energie od spoločnosti Huawei
„Pokiaľ ide o architektúru, veríme, že dvojstupňové riešenie ponúka v porovnaní s konvenčným jednostupňovým riešením vynikajúcu bezpečnosť siete," hovorí Steve Zheng.Po
More news about: Huawei
Jul 15, 2026, 13:59 ET SpinaFX Medical Receives CE Mark MDR Certification for its Triojection® System, Expanding Access to Minimally Invasive Lumbar Disc Treatment Across Europe and Key International Markets
Administration's (FDA's) award of a Breakthrough Device Designation for Triojection in 2025. Triojection has also received an FDA Investigational Device Exemption (IDE), which permits SpinaFX to proceed with a clinical trial evaluating image‑guided intradiscal ozone‑oxygen injection for contained herniated lumbar discs.
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Jul 15, 2026, 11:13 ET Silné výsledky strategického upgradu značky GENMA - množstvo významných objednávok a globálne uznanie automatizačnej technológie
kusovAutomatizačná platforma GENSMART značky GENMA zahŕňa základné riešenia vrátane systémov AutoRTG, AutoRMG, AutoSTS a ovládacích systémov zariadení. Ide o konvergenciu špičkových technológií vrátane multimodálnej fúzie údajov zo senzorov, možnosti vzájomnej výmeny údajov medzi systémami, koordinovaného
More news about: RAINBOWCO
Jul 15, 2026, 10:00 ET Voice-to-Text Was Never Enough. Meet Voice That Sees.
already use it to varying degrees. The honest distinction is depth — Loqua goes deep on the desktop, making stronger assumptions about your editor, your IDE, and the apps you actually work in all day.From hearing to understandingVoice typing is graduating from a transcription
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Jul 14, 2026, 10:00 ET Mercantile Community Partners Reaches 500 Affordable Housing Units Financed Across Michigan
to community development investment.The Flats on Bridge development was undertaken by Homestretch Nonprofit Housing Corporation and IDE Development, organizations dedicated to creating quality affordable housing opportunities in Michigan communities."Affordable housing is essential
More news about: Mercantile Bank Corporation
Jul 14, 2026, 08:49 ET "Now is Your Moment": Huawei Hadirkan Berbagai Potensi Baru untuk Setiap Momen Lewat Inovasi yang Mencakup Seluruh Skenario
HUAWEI MatePad Air dengan kemampuan produktivitas setara PC serta berbagai fitur berbasis AI yang membantu pengguna bekerja lebih efisien, mengembangkan ide menjadi konten, dan menyusun berbagai materi presentasi dengan lebih mudah. Melalui perpaduan antara perangkat keras dan perangkat lunak tersebut, pengguna
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Jul 14, 2026, 05:00 ET Newronika Receives CE Mark for αDBS®, Advancing Its Mission to Make Adaptive Therapy the Standard of Care
centers.Advancing Toward U.S. FDA Approval: The ADVENT Pivotal TrialAlongside its European CE Mark, Newronika holds an Investigational Device Exemption (IDE) from the United States FDA, enabling the ADVENT pivotal trial, a study spanning the United States and the European Union, designed to support FDA approval
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Jul 14, 2026, 05:00 ET Newronika Receives CE Mark for αDBS®, Advancing Its Mission to Make Adaptive Therapy the Standard of Care
centers.Advancing Toward U.S. FDA Approval: The ADVENT Pivotal TrialAlongside its European CE Mark, Newronika holds an Investigational Device Exemption (IDE) from the United States FDA, enabling the ADVENT pivotal trial, a study spanning the United States and the European Union, designed to support FDA approval
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Jul 10, 2026, 13:22 ET Spoločnosť DJI testuje drony na najvyššom vrchole sveta, čím zdokonaľuje kritické aplikácie pre doručovanie vo vysokých nadmorských výškach, mapovanie a výskum klímy
zameraniu na bezpečnosť horolezectva v reálnom čase," povedal Raj Bikram Maharjan, generálny riaditeľ spoločnosti Airlift Technology. „Pokiaľ vieme, ide o prvé nasadenie svojho druhu v Nepále a potenciálne jedno z prvých reálnych prevádzkových využití na celom svete v tomto rozsahu v prostredí expedícií
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Jul 09, 2026, 17:41 ET Vťahujeme fanúšikov do hry: Hisense prináša počas Majstrovstiev sveta vo futbale FIFA World Cup 2026™ lepší zážitok zo sledovania inováciami v oblasti zobrazovania
Či už ide o intenzitu gólu v poslednej chvíli, atmosféru na štadióne alebo každý jemný pohyb na ihrisku, technológie Hisense sú navrhnuté tak, aby priblížili divákov
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Jul 09, 2026, 06:00 ET Data Center Water & Wastewater Treatment Equipment Market worth $5.90 billion by 2031 - Exclusive Report by MarketsandMarkets™
Lenntech B.V. (Netherlands), IDE (Israel).Get access to the latest updates on
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Jul 08, 2026, 04:28 ET AiPPT.com Lengkapi Ekosistem Presentasi Berbasis AI dengan Empat Mode Terintegrasi dan Alur Kerja yang Lebih Cerdas
templat, serta komponen interaktif yang dapat menyesuaikan perkembangan ide.Di sisi lain, AiPPT Visual memperkuat kemampuan visual storytelling melalui integrasi
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Jul 06, 2026, 10:46 ET Global Neurotechnology Market is Projected to Cross USD 50 Billion by 2034 | DelveInsight
brain-computer interface (BCI) company focused on advancing mental health technologies, received approval from the FDA for an Investigational Device Exemption (IDE) to initiate the RESONATE Early Feasibility Study.In March 2026, China approved the world's first commercial brain-computer interface
More news about: DelveInsight Business Research, LLP
Jul 06, 2026, 09:25 ET Aethlon Medical Announces Pricing of $4.0 Million Follow-On Offering Priced At-The-Market Under NASDAQ Rules
development or severity of the disease. The Hemopurifier also holds an FDA Breakthrough Device designation and an open Investigational Device Exemption (IDE) application related to the treatment of life-threatening viruses that are not addressed with approved therapies.Additional information can be
More news about: Aethlon Medical, Inc.
Jul 06, 2026, 08:00 ET Bamboo Insurance Introduces Essential Homeowners Program Focused on Core Coverage Needs
expand efficiently in existing and new markets while delivering value to policyholders, underwriting partners, and distribution partners.Bamboo Ide8 Insurance Services, LLC. ("Bamboo Insurance") is Managing General Agency licensed to sell property-casualty insurance products; NPN 18657046; CA License
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Jul 02, 2026, 20:00 ET JINRO, svetová jednotka v kategórii nápojov soju, ohlasuje partnerstvo s V zo skupiny BTS
vedúcom postavení a dedičstve, ktoré si značka vybudovala.O značke JINROZnačka JINRO bola prvýkrát uvedená na trh v roku 1924. Ide o kórejskú reprezentatívnu značku nápojov soju, svetovú jednotku v oblasti soju a najpredávanejšiu značku liehovín na svete. JINRO oslovuje spotrebiteľov
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Jul 02, 2026, 09:00 ET Manycore Tech Announces Three Papers Accepted to ECCV 2026, Unveiling Full-Stack Infrastructure for Physical AI
Syn-GRPO tackles the fundamental scarcity of diverse 3D training data through a self-evolving data framework; and WalkerBench, paired with the Spatial-IDE framework, establishes the field's first rigorous real-world benchmark for spatial navigation — and closes the loop from evaluation to physical deployment.A
More news about: Manycore Tech Inc.
Jul 01, 2026, 07:08 ET Reju otvára v Conshohockene v Pensylvánii prvé americké centrum výskumu a vývoja
z výskumného centra Almaden spoločnosti IBM v San Jose v Kalifornii, kde bola prvýkrát vyvinutá technológia depolymerizácie Volcat spoločnosti Reju. Ide o katalytickú chemickú recyklačnú metódu rozkladu polyesteru na opakovane použiteľné suroviny.„Som nadšený, že sa môžem pripojiť k takejto inovatívnej
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Jun 30, 2026, 17:02 ET LINE V ATÉNACH VYHLÁSENÝ ZA NO.1 PRI ODHALENÍ PRVÉHO ZOZNAMU EUROPE'S 50 BEST BARS 2026
Poland. Super Lyan (No.42) vyhráva cenu The Best Bar in the Netherlands, sponzoruje Ketel One. Late Bloomers sa umiestnil na mieste No.44 a ide o The Best Bar in Switzerland, sponzorované Amaro Lucano, zatiaľ čo Dunlin je na mieste No.50 v kategórii The Best Bar in Austria.Kontakt
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Jun 29, 2026, 19:00 ET Laplace Announces FDA IDE Approval of TRIUMPH Pivotal Trial of Its Transcatheter Tricuspid Valve Replacement System
/PRNewswire/ -- Laplace Interventional today announced that the U.S. Food and Drug Administration (FDA) has approved an Investigational Device Exemption (IDE) for TRIUMPH, the company's pivotal trial evaluating its Transcatheter Tricuspid Valve Replacement (TTVR) system.
More news about: Laplace Interventional, Inc.
Jun 29, 2026, 07:08 ET Antier Sets a New Global Standard for Blockchain Development - Every Layer, Every Industry, One Partner
Ethereum, EVM-compatible chains, and Wasm environments under a single unified network - complete with a decentralized VPN, an AI-powered smart contract IDE (QubeQode), and MPC-secured cross-chain infrastructure.The Next Frontier: AI, Blockchain, and the Infrastructure of TomorrowThe
More news about: Antier Solutions
Jun 29, 2026, 07:00 ET Artivion Announces U.S. FDA Approval of the AMDS Hybrid Prosthesis
device preserves the native arch, enabling minimally invasive re-interventions if needed. The PMA approval is based on data from the PERSEVERE U.S. IDE trial, which at 30 days demonstrated a 72% reduction in all-cause mortality and a 54% reduction in primary major adverse events (MAEs), including stroke,
More news about: Artivion, Inc.