PRECO, LLC

FDA Device Registration & Listing · Somerset, WI, US · Registration 3005857283

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
3005857283
FEI Number
3005857283
Entity Name
PRECO, LLC
City/State/Country
Somerset, WI, US
Establishment Address
500 Laser Dr, Somerset, WI 54025, US
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Preco, LLC (Owner Number: 10094658)
Owner / Operator Contact Address
500 Laser Drive, Somerset, WI 54025, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ScarAway

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 2025-12-14

Official Correspondent

Thomas Goeltl

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Preco, 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 3005857283. Last updated year: 2026. Please use registration number 3005857283 when referencing this establishment in official correspondence.
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