PROCELL THERAPIES, LLC

FDA Device Registration & Listing · Austin, TX, US · Registration 3011193532

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
3011193532
FEI Number
3011193532
Entity Name
PROCELL THERAPIES, LLC
City/State/Country
Austin, TX, US
Establishment Address
8868 Research Blvd, Austin, TX 78758, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ProCell Therapies, LLC (Owner Number: 10047699)
Owner / Operator Contact Address
877 BAY ESPLANADE, Clearwater Beach, FL 33767, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Procell Therapies

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GFE Brush, Dermabrasion, Powered General, Plastic Surgery Class 1 878.4820 2014-10-21

Official Correspondent

Mitchell Schwartz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ProCell Therapies, 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 3011193532. Last updated year: 2026. Please use registration number 3011193532 when referencing this establishment in official correspondence.
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