Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3038014307

FEI Number

3038014307

Entity Name

CURAPEP LLC

City/State/Country

Burlington, WI, US

Establishment Address

W1001 Honey Creek Rd, Burlington, WI 53105, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Curapep LLC (Owner Number: 10093225)

Owner / Operator Contact Address

W1001 Honey Creek Rd., Burlington, WI 53105, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

VityPatch

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NAE	Dressing, Wound, Hydrogel Without Drug And/Or Biologic	General, Plastic Surgery	Class 1	878.4022	2025-04-15

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Curapep 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 3038014307. Last updated year: 2026. Please use registration number 3038014307 when referencing this establishment in official correspondence.