VERSIPEL, LLC

FDA Device Registration & Listing · Dunmore, PA, US · Registration 3019682549

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
3019682549
FEI Number
3019682549
Entity Name
VERSIPEL, LLC
City/State/Country
Dunmore, PA, US
Establishment Address
201 South Blakely Street, #324, Dunmore, PA 18512, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Sanguine Technology, LLC (Owner Number: 10082245)
Owner / Operator Contact Address
201 South Blakely Street, #324, Dunmore, PA 18512, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

D-Ostomy

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EZS Appliance, Colostomy, Disposable Gastroenterology, Urology Class 1 876.5900 2021-06-30

Official Correspondent

Gregory Murphy

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Sanguine Technology, 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 3019682549. Last updated year: 2026. Please use registration number 3019682549 when referencing this establishment in official correspondence.
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