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The Syntech Chronos 68 is a highly customizable magnetic switch keyboard that, with some small Mac-specific issues aside, is ...
Cronos: The New Dawn amps up tension with a deadly Merge mechanic—enemies evolve mid-battle by absorbing corpses. Learn how to survive the chaos.
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TheGamer on MSNChrono Odyssey Class And Combat GuideChrono Odyssey is an upcoming action-combat MMO, developed by Chrono Studio - a new studio composed of South Korean MMO ...
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Comics Gaming Magazine on MSNCronos: The New Dawn Brings Bloober’s Darkest Vision Yet to Game Con CanadaThe New Dawn at Game Con Canada. An ambitious horror game set in 1980s Poland, where time travel and flesh-melding monsters fuel a chilling new direction.
LOT OF FUN OUT THERE, CHRISTINA. AND WE CAN SEE IT. ALL RIGHT, IN CASE YOU NEED A RECAP OF THE STORY BEHIND THIS NEW THEME PARK, IT ALL STARTS WITH THE CHRONOS. THIS MASSIVE DEVICE SITS AT THE ...
Activision’s Legal Action. On May 8, 2025, Activision sent a cease and desist letter to the Cronus Zen manufacturer, telling them to stop selling these devices—or else face court.
Cronus is in the center of a debate between cheating and accessibility. Transparently, Cronus’ devices can be used so that players can get an advantage over others in online games.
Call of Duty Targets Cronus and Other Third-Party Hardware That Allows Cheating call of duty: black ops 6 PlayStation has made efforts to block these kinds of devices , but it only goes so far.
TORONTO, May 08, 2025 (GLOBE NEWSWIRE) -- Cronos Group Inc. (NASDAQ: CRON) (TSX: CRON) (“Cronos” or the “Company”), today announced its 2025 first quarter business results. "2025 is ...
Cronos: The New Dawn leads an issue that travels all over Europe. In Paris we find Sifu developer Sloclap working on Rematch, an unexpected pivot into football that retains the studio’s ...
BORDEAUX, France & SAN DIEGO, September 04, 2024--Germitec, an innovative French MedTech company specializing in High-Level Disinfection (HLD) for ultrasound probes through its unique proprietary ...
Through the De Novo classification process, FDA concludes that this device should be regulated under Regulation Number 21 CFR 880.6511 and classified as a Class II medical device.
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