FETTECH

FDA Device Registration & Listing · Davie, FL, US · Registration 3014498807

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
3014498807
FEI Number
3014498807
Entity Name
FETTECH
City/State/Country
Davie, FL, US
Establishment Address
12040 Ashford Ln, Davie, FL 33325, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
FetTech (Owner Number: 10088070)
Owner / Operator Contact Address
12040 Ashford Ln, Davie, FL 33325, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K172593
PMA Number
N/A

All Registered Proprietary Names

REYAGEL XCelliStem

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGN Wound Dressing With Animal-Derived Material(S) Unknown Class U N/A 2025-11-26
KGN Wound Dressing With Animal-Derived Material(S) Unknown Class U N/A 2023-05-22

Official Correspondent

Clay Fette

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FetTech
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K112888 Kensey Nash Corporation MESO WOUND MATRIX 2012-02-10
K040211 Collagen Matrix, Inc. MODIFICATION TO: COLLAGEN TOPICAL WOUND DRESSING 2004-02-27

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014498807. Last updated year: 2026. Please use registration number 3014498807 when referencing this establishment in official correspondence.
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