SPACEBANDER CORPORATION

FDA Device Registration & Listing · Hillsborough, NJ, US · Registration 3013681539

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
3013681539
FEI Number
3013681539
Entity Name
SPACEBANDER CORPORATION
City/State/Country
Hillsborough, NJ, US
Establishment Address
120 Stryker Lane, Suite 104, Hillsborough, NJ 08844, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SpaceBander Corporation (Owner Number: 10054787)
Owner / Operator Contact Address
120 Stryker Lane, Suite 104, Hillsborough, NJ 08844, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SpaceBander

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FHN Ligator, Hemorrhoidal Gastroenterology, Urology Class 2 876.4400 2017-04-26

Official Correspondent

Howard Loonan

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SpaceBander Corporation
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
K000397 Boston Scientific Corp SPEEDBAND SUPERVIEW MULTIPLE BAND LIGATOR, MODELS 4225, 4228; INJECTION SPEEDBAND SUPERVIEW MULTIPLE BAND LIGATOR, MODEL 2000-03-07

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013681539. Last updated year: 2026. Please use registration number 3013681539 when referencing this establishment in official correspondence.
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