INTEPROD LLC

FDA Device Registration & Listing · Eagleville, PA, US · Registration 3007204745

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
3007204745
FEI Number
3007204745
Entity Name
INTEPROD LLC
City/State/Country
Eagleville, PA, US
Establishment Address
2583 Industry Ln, Eagleville, PA 19403, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Inteprod LLC (Owner Number: 10029843)
Owner / Operator Contact Address
2583 Industry Ln, Eagleville, PA 19403, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Dental GoScope DVS1000; Surgical GoScope DVSA2010; Teaching GoScope DVSA3000 Infrascanner Model 2000

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EPT Microscope, Surgical General, Plastic Surgery Class 1 878.4700 2025-08-21
OPT Infrared Hematoma Detector Ophthalmic Class 2 882.1935 2013-01-21

Official Correspondent

Suzanne Smethers

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Inteprod 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 3007204745. Last updated year: 2026. Please use registration number 3007204745 when referencing this establishment in official correspondence.
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