LV Liberty Vision

FDA Device Registration & Listing · Portsmouth, NH, US · Registration 3015042204

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
3015042204
FEI Number
3015042204
Entity Name
LV Liberty Vision
City/State/Country
Portsmouth, NH, US
Establishment Address
300 West Rd Ste 2, Portsmouth, NH 03801, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
LV Liberty Vision (Owner Number: 10059015)
Owner / Operator Contact Address
300 West Road, Unit 2, Portsmouth, NH 03801, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K193602
PMA Number
N/A

All Registered Proprietary Names

LV iWand A6 LV iWand A Assembly Stand Liberty Vision iWand Anterior Applicator Assembly Stand for Liberty Vision Yttrium-90 Discs Liberty Vision iWand Posterior Applicator - 6 mm LV iWand P Assembly Stand LV iWand P6 Liberty Vision iWand Posterior Applicator Assembly Stand for Liberty Vision Yttrium-90 Discs Liberty Vision iWand Anterior Applicator - 6 mm LV iWand A10 Liberty Vision iWand Posterior Applicator - 10 mm Liberty Vision iWand Anterior Applicator - 10 mm LV iWand P10 Liberty Vision Yttrium-90 Disc - 6 mm LV Y-90 D6 LV Liberty Vision Model 1 90Yttrium Brachytherapy Source LV Y-90 D10 Liberty Vision Yttrium-90 Disc - 10 mm

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IWJ System, Applicator, Radionuclide, Manual Radiology Class 1 892.5650 2021-11-30
KXK Source, Brachytherapy, Radionuclide Radiology Class 2 892.5730 2021-11-30

Official Correspondent

Kyle Mohney

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LV Liberty Vision
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
K973037 Avid N.I.T., Inc. N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000 1998-01-27

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0040-2012 Worldwide Medical Technologies, LLC 1
Prostrate Seeding Applicator Needle. Product code PSS1820AT Packed in boxes of (25) with five Single Packs and four five packs or as singles or five packs. Worldwide Medical Technologies, LLC Used to introduce radionuclide seeds of 1-125 or Pd-103 into the body for radiation therapy. This device is typically used in the transperineal approach for placing radionuclide seeds in the prostate

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015042204. Last updated year: 2026. Please use registration number 3015042204 when referencing this establishment in official correspondence.
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