IMPLANT RESOURCE, INC.

FDA Device Registration & Listing · Eagan, MN, US · Registration 2184171

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
2184171
FEI Number
1000139815
Entity Name
IMPLANT RESOURCE, INC.
City/State/Country
Eagan, MN, US
Establishment Address
917 Lone Oak Rd, Suite 1000, Eagan, MN 55121, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
IMPLANT RESOURCE, INC dba MEDICAL PRODUCTS RESOURCE (Owner Number: 9010087)
Owner / Operator Contact Address
917 Lone Oak Rd, Suite 1000, --, Eagan, MN 55121, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MPR Pins SURGIPRESS TOURNIQUET MPR-11200-1000

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HTY Pin, Fixation, Smooth Orthopedic Class 2 888.3040 2022-05-23
KCY Tourniquet, Pneumatic General, Plastic Surgery Class 1 878.5910 2003-09-17
HXL Mallet General, Plastic Surgery Class 1 878.4800 2021-08-09

Official Correspondent

MICHAEL HOLLOWAY

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

IMPLANT RESOURCE, INC dba MEDICAL PRODUCTS RESOURCE
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
K895079 Buckman Co., Inc. ACE BEADED K-WIRES ACE OLIVE WIRES 1989-09-13
K922193 Osteo AG OSTEO KIRSCHNER WIRE 1992-07-23
K850026 Kirkstil Corp., Inc. ORTHOPEDIC IMPLANT NAILS & PINS 1985-05-20
K963367 Rms Div. RMS K-WIRE 1996-10-30

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0013-05 Biomet, Inc. 2
Lactosorb pin, 2.0 x 20 mm, sterile; ref. 948205.

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8043862 AAP IMPLANTATE AG BERLIN, DE
3006783837 STRUCTURE MEDICAL, LLC. Naples, FL, US
3015231789 Arthrex Manufacturing Inc. Pendleton, SC, US
2029275 Sterigenics U.S., LLC Corona, CA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2184171. Last updated year: 2026. Please use registration number 2184171 when referencing this establishment in official correspondence.
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