Route 92 Medical, West Jordan

FDA Device Registration & Listing · W Jordan, UT, US · Registration 3030088112

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
3030088112
FEI Number
3030088112
Entity Name
Route 92 Medical, West Jordan
City/State/Country
W Jordan, UT, US
Establishment Address
1375 W 8040 S, W Jordan, UT 84088, US
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
Route 92 Medical (Owner Number: 10054934)
Owner / Operator Contact Address
155 Bovet Road, Suite 100, San Mateo, CA 94402, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

FreeClimb 54 Reperfusion Catheter with Tenzing 5 FreeClimb 54 Reperfusion System HiPoint reperfusion catheter with Tenzing FreeClimb 70 reperfusion catheter with Tenzing 7

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NRY Catheter, Thrombus Retriever Cardiovascular Class 2 870.1250 2024-05-17
NRY Catheter, Thrombus Retriever Cardiovascular Class 2 870.1250 2025-05-23
QJP Catheter, Percutaneous, Neurovasculature Cardiovascular Class 2 870.1250 2021-11-01
DQY Catheter, Percutaneous Cardiovascular Class 2 870.1250 2019-07-11
NRY Catheter, Thrombus Retriever Cardiovascular Class 2 870.1250 2023-04-25

Official Correspondent

Matthew Fortson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Route 92 Medical
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3016522967 Route 92 Medical, Head Quarters San Mateo, CA, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K033736 Concentric Medical, Inc. MERCI RETRIEVER, MODELS 90065, 90066 2004-08-11
K043580 Chestnut Medical Technologies, Inc. ALLIGATOR RETRIEVAL DEVICE (ARD) 2005-03-24
K982883 Medtronics Interventional Vascular MEDTRONIC 7F AND 8F ZUMA GUIDING CATHETER 1998-09-04
K132420 Reflow Medical WINGMAN EXTENDABLE TIP SUPPORT CATHETER 2013-09-19
K082339 Endocross, Ltd. ENABLER-P SUPPORT CATHETER 2008-11-20

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0021-2025 Stryker Neurovascular 2
The Trevo Trak 21 Microcatheter is a single-lumen, braided shaft, variable stiffness catheter with radiopaque marker(s) on the distal end and a luer hub on the proximal end. The catheter shaft has a hydrophilic coating on the distal 100cm to reduce friction during use. The radiopaque shaft and distal marker(s) facilitate fluoroscopic visualization. A rotating hemostatic valve with side-arm adapter is provided with each microcatheter.
Z-0001-2010 Penumbra Inc. 2
Penumbra Neuron Delivery Catheter 070, percutaneous catheter, catalog numbers PND6F0701058, PND6F070956, PND6F0701058M, and PND6F070956M; manufactured by Penumbra, Inc., Alameda, CA. Indicated for the introduction of interventional devices into the peripheral, coronary, and neuro vasculature.
Z-0003-2014 Cordis Corporation 2
Cordis ADROIT 6F Guiding Catheter Product Usage: For intravascular introduction of interventional and/or diagnostic devices into the coronary or peripheral vascular system.
Z-0009-2024 Boston Scientific Corporation 2
Guider Softip Guide Catheter 6F PRE-SHAPED 40 90CM, Catalog number H965100420, cardiac guide catheter
Z-0010-04 Bard Peripheral Vascular 2
Conquest Balloon Dilation Catheters Model/Catalog Number CQ 75124

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030088112. Last updated year: 2026. Please use registration number 3030088112 when referencing this establishment in official correspondence.
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