I can assure you, as a former quality engineer at a medical device development facility, that there is absolutely, positively zero chance that anyone there will use any AI-powered coding tools to write code that goes onto any device that is ISO-13485, CE, or otherwise compliant to some existing medical device regulations (I speak in the USA and European markets; I cannot speak for other markets). There is literally a defined waterfall development cycle for FDA-regulated devices that requires software features to be very precisely specified, implemented, validated, tested, and manufactured. Anyone suggesting using AI at such a facility would be laughed out of the room, and perhaps even re-trained on the procedures. Anyone caught using such tools would probably be fired immediately and all their code patches would be put under intense scrutiny and possibly even rewritten; of course the device software they were working on would remain in development and not released until that was fixed.