VIV FOR YOUR V, INC.

FDA Device Registration & Listing · Boston, MA, US · Registration 3017978050

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
3017978050
FEI Number
3017978050
Entity Name
VIV FOR YOUR V, INC.
City/State/Country
Boston, MA, US
Establishment Address
50 Terminal Street, Building 2 Suite 416, Boston, MA 02129, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
VIV FOR YOUR V, INC. (Owner Number: 10079634)
Owner / Operator Contact Address
85 Seaport Blvd, Apt 510, Boston, MA 02210, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HHE Cup, Menstrual Obstetrics/Gynecology Class 2 884.5400 2020-12-17
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2020-12-17

Official Correspondent

Katie Diasti

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VIV FOR YOUR V, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K823241 Kimberly-Clark Corp. NEW FREEDOM THIN UNSCENTED MAXI PADS 1982-12-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017978050. Last updated year: 2026. Please use registration number 3017978050 when referencing this establishment in official correspondence.
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