NOVOCURE INC

FDA Device Registration & Listing · Portsmouth, NH, US · Registration 3009306483

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
3009306483
FEI Number
3009306483
Entity Name
NOVOCURE INC
City/State/Country
Portsmouth, NH, US
Establishment Address
195 Commerce Way, Portsmouth, NH 03801, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
NOVOCURE INC (Owner Number: 10040460)
Owner / Operator Contact Address
1550 Liberty Ridge Dr, Suite 115, Wayne, PA 19087, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P230042

All Registered Proprietary Names

Optune Treatment Kit Transducer Array Optune Pax Optune Lua

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NZK Stimulator, Low Electric Field, Tumor Treatment Unknown Class 3 N/A 2012-04-17
SHC Low Electric Field Generator For Pancreatic Cancer Treatment Unknown Class 3 N/A 2026-02-18
SDA Electrical Tumor Treatment Fields For Non-Small Cell Lung Cancer Unknown Class 3 N/A 2024-12-13

Official Correspondent

Lori Burns

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NOVOCURE INC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009306483. Last updated year: 2026. Please use registration number 3009306483 when referencing this establishment in official correspondence.
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