STAR PORT INC

FDA Device Registration & Listing · Denver, CO, US · Registration 3036035308

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
3036035308
FEI Number
3036035308
Entity Name
STAR PORT INC
City/State/Country
Denver, CO, US
Establishment Address
835 JASMINE ST, Denver, CO 80220, US
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Star Port Inc (Owner Number: 10092674)
Owner / Operator Contact Address
835 JASMINE ST, Denver, CO 80220, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Silicone Scar Gel, Silicone Scar Sheets (SC-03) Hydrogel Dressing (HD-05) Scar Gel (SG-03)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MDA Elastomer, Silicone, For Scar Management General, Plastic Surgery Class 1 878.4025 2025-02-05
NAE Dressing, Wound, Hydrogel Without Drug And/Or Biologic General, Plastic Surgery Class 1 878.4022 2026-02-05
PFP Silicone Hydrogel For Scar Management General, Plastic Surgery Class 1 878.4025 2025-12-25

Official Correspondent

Emma Tapia

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Star Port Inc
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 3036035308. Last updated year: 2026. Please use registration number 3036035308 when referencing this establishment in official correspondence.
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