VYCOR MEDICAL INC

FDA Device Registration & Listing · Boca Raton, FL, US · Registration 3005880844

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3005880844
FEI Number
3005880844
Entity Name
VYCOR MEDICAL INC
City/State/Country
Boca Raton, FL, US
Establishment Address
951 BROKEN SOUND PKWY STE 320, Boca Raton, FL 33487, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
VYCOR MEDICAL INC (Owner Number: 9085664)
Owner / Operator Contact Address
951 Broken Sound Pkwy, Suite 320, Boca Raton, FL 33487, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K060973
PMA Number
N/A

All Registered Proprietary Names

VYCOR VIEWSITE SUR

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GZT Retractor, Self-Retaining, For Neurosurgery Neurology Class 2 882.4800 2006-08-17

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VYCOR MEDICAL INC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Other Registrations for Same Entity

Registration Number Establishment Name Location
3004594297 NOVAVISION, INC. BOCA RATON, FL, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005880844. Last updated year: 2026. Please use registration number 3005880844 when referencing this establishment in official correspondence.
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