LaunchPort LLC

FDA Device Registration & Listing · Baltimore, MD, US · Registration 3015259858

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
3015259858
FEI Number
3015259858
Entity Name
LaunchPort LLC
City/State/Country
Baltimore, MD, US
Establishment Address
101 West Dickman St. Suite 900, Baltimore, MD 21230, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
LaunchPort LLC (Owner Number: 10083736)
Owner / Operator Contact Address
101 West Dickman St, Suite 900, Baltimore, MD 21230, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

eNeura

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGC Tube, Gastro-Enterostomy Gastroenterology, Urology Class 2 876.5980 2024-04-18
KTH Device, Anti-Stammering Ear, Nose, Throat Class 1 874.5840 2021-12-15
OKP Transcranial Magnetic Stimulator For The Treatment Of Migraine Headache Neurology Class 2 882.5808 2021-12-15
ESE Larynx, Artificial (Battery-Powered) Ear, Nose, Throat Class 1 874.3375 2021-12-15

Official Correspondent

Bob Storey

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LaunchPort LLC
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 3015259858. Last updated year: 2026. Please use registration number 3015259858 when referencing this establishment in official correspondence.
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