JFD-PK MEDICAL LLC

FDA Device Registration & Listing · Center Valley, PA, US · Registration 3024792425

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
3024792425
FEI Number
3024792425
Entity Name
JFD-PK MEDICAL LLC
City/State/Country
Center Valley, PA, US
Establishment Address
4400 Cumorah Ave, Center Valley, PA 18034, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
JFD-PK Medical LLC (Owner Number: 10088142)
Owner / Operator Contact Address
4400 Cumorah Ave, Center Valley, PA 18034, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Durrani Silicone Chest Tube Kit, JD-3000 Durrani General Purpose Silicone Drainage Catheter Kit, JD-2000

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GBA Catheter, Balloon Type General, Plastic Surgery Class 1 878.4200 2024-03-30

Official Correspondent

Jameel Durrani

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

JFD-PK Medical LLC
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 3024792425. Last updated year: 2026. Please use registration number 3024792425 when referencing this establishment in official correspondence.
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