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Extra Security helps medical device manufacturers get through FDA cybersecurity review — faster, cleaner, and without surprises. We do two things exceptionally well: penetration testing and threat modeling for connected medical devices. Your device ships to our hardware lab, where our team tests network protocols, firmware, physical interfaces, and cloud components the way a real attacker would. You get back a report mapped to FDA premarket cybersecurity guidance, ready to drop into your 510(k) or PMA submission. Every engagement includes: - 4-week turnaround from device receipt to final report - FDA-compliant deliverables (executive summary, methodology, findings with proof-of-concept, risk assessment, remediation roadmap) - One free re-test within 60 days - Transparent, upfront pricing — no scoping games We also help manufacturers respond to FDA ANIN cybersecurity letters, validate equivalency claims for substantial-equivalence submissions, and build custom engagements for unusual devices or testing scopes.

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Alberto Correa is the Gerente general of ExtraSecurity.

2 people are employed at ExtraSecurity.

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