AccuVein Inc.

FDA Device Registration & Listing · Medford, NY, US · Registration 3007121351

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
3007121351
FEI Number
3007121351
Entity Name
AccuVein Inc.
City/State/Country
Medford, NY, US
Establishment Address
3243 Route 112, Building 1, Suite 2, Medford, NY 11763, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
AccuVein, Inc. (Owner Number: 10026504)
Owner / Operator Contact Address
3243 Route 112, Building 1, Suite 2, Medford, NY 11763, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

AV600 AV400 HF580 Hands-Free Powered Goose Neck Wheeled Stand AV300 AccuVein HF510 Hands-Free Stand AccuVein HF550 Hands-Free Stand AV500

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KZA Device, Vein Location, Liquid Crystal General Hospital Class 1 880.6970 2008-07-23

Official Correspondent

David Martin

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AccuVein, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3009964638 AccuVein Inc. San Jose, CA, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007121351. Last updated year: 2026. Please use registration number 3007121351 when referencing this establishment in official correspondence.
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