FR TECH, LLC

FDA Device Registration & Listing · Springboro, OH, US · Registration 3042750477

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
3042750477
FEI Number
3042750477
Entity Name
FR TECH, LLC
City/State/Country
Springboro, OH, US
Establishment Address
195 Advanced Dr, Springboro, OH 45066, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
FR Tech, LLC (Owner Number: 10094689)
Owner / Operator Contact Address
195 Advanced Dr, Springboro, OH 45066, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K910944
PMA Number
N/A

All Registered Proprietary Names

CURCO 2" x 2" Collagen Sheet CURCO 1" x 10" Collagen Sheet CURCO 4" x 4" Collagen Sheet CURCO 1" x 1" Collagen Sheet CURCO 1" x 4" Collagen Sheet CURCO 7" x 7" Collagen Sheet CURCO 2" x 10" Collagen Sheet Curco Silcur CURCO Collagen Particles 1g

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 2026-02-17
FQM Bandage, Elastic General Hospital Class 1 880.5075 2025-12-16
KGN Wound Dressing With Animal-Derived Material(S) Unknown Class U N/A 2026-02-17

Official Correspondent

Rob Jarrell

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FR Tech, LLC
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 3042750477. Last updated year: 2026. Please use registration number 3042750477 when referencing this establishment in official correspondence.
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