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Akins P
@akinsproven
FDA Regulatory Affairs Specialist, Medical Device 510k Strategist
Nigeria
English
About me
I am Akins Proven, an FDA Regulatory Affairs Specialist accelerating US market clearance for MedTech innovators, hardware startups, and global manufacturers. Specializing in 21 CFR, 510(k) dossiers, predicate mapping, and classification pathways, I de-risk commercialization across Class I/II and SaMD devices. I translate intricate FDA CDRH rules into audit-ready documentation that eliminates Refuse-to-Accept (RTA) risk. Fast, defensible, and investor-ready. Message me with your device concept to lock in your US regulatory clearance strategy today.
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Akins P
Offline •
See my services
Medical Device Regulatory
I will research fda predicate devices for your medical device 510k submission
Medical Device Regulatory
I will research your fda medical device classification and product code
