STRATUS MEDICAL

FDA Device Registration & Listing · Magnolia, TX, US · Registration 3017423051

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
3017423051
FEI Number
3017423051
Entity Name
STRATUS MEDICAL
City/State/Country
Magnolia, TX, US
Establishment Address
32303 FM 2978 Rd, Magnolia, TX 77354, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Stratus Medical (Owner Number: 10077915)
Owner / Operator Contact Address
32303 FM 2978 Rd, Magnolia, TX 77354, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Vesta RF Cannula MINTA RYAN RF THERMOCOUPLE ELECTRODE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GXI Probe, Radiofrequency Lesion Neurology Class 2 882.4725 2020-10-05
GXI Probe, Radiofrequency Lesion Neurology Class 2 882.4725 2021-03-19

Official Correspondent

Lisa Pelletier

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Stratus Medical
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
K253907 ABBOTT MEDICAL Disposable Radiofrequency Cannula 2026-04-16
K242841 ABBOTT MEDICAL Disposable RF Electrode (RFDE-5/RFDE-10/RFDE-15/RFDE-20) 2025-05-27

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0720-2020 Abbott Medical 2
CLASSIC Radiofrequency Cannula - Curved, 10 cm, SMK Compatible Electrode, REF C-1005-S - Product Usage: Disposable Radiofrequency Cannulae are provided in either straight, curved, or curved blunt geometries with a stylet inserted in the cannula. Cannulae are insulated except for the active tip. The active tip determines the size of the radiofrequency lesion.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017423051. Last updated year: 2026. Please use registration number 3017423051 when referencing this establishment in official correspondence.
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