NEW LANTERN

FDA Device Registration & Listing · San Francisco, CA, US · Registration 3036039341

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
3036039341
FEI Number
3036039341
Entity Name
NEW LANTERN
City/State/Country
San Francisco, CA, US
Establishment Address
1050 Sansome St Ste 400, San Francisco, CA 94111, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
New Lantern (Owner Number: 10090066)
Owner / Operator Contact Address
1050 Sansome, Suite 400, San Francisco, CA 94111, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

New Lantern Platform Curie

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LMD System, Digital Image Communications, Radiological Radiology Class 1 892.2020 2024-02-09

Official Correspondent

Shiva Suri

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3036039341. Last updated year: 2026. Please use registration number 3036039341 when referencing this establishment in official correspondence.
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