SPINOLOGICS, INC. also DBA Spino Modulation Inc and Numalogics Inc

FDA Device Registration & Listing · Montreal Quebec, CA · Registration 3010806484

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
3010806484
FEI Number
3010806484
Entity Name
SPINOLOGICS, INC. also DBA Spino Modulation Inc and Numalogics Inc
City/State/Country
Montreal Quebec, CA
Establishment Address
4200 Boulevard Saint-Laurent, Suite 1100, Montreal Quebec H2W 2R2, CA
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Spinologics, Inc. (Owner Number: 10046275)
Owner / Operator Contact Address
4200 boulevard Saint-Laurent, Local 1100, Montreal, CA-QC H2W 2R2, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MIThoraTM Trocar

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LXH Orthopedic Manual Surgical Instrument Orthopedic Class 1 888.4540 2024-02-09

Official Correspondent

Marc-Andre Cote

US Agent Details

Elisa D. Harvey, DVM, PhD Business: CardioMed Device Consultants LLC Email: eharvey@cardiomedllc.com Phone: (410) 6742060

Related Public Records

Same Entity

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

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0009-2007 Smith & Nephew Inc 1
Journey Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 74018811, 74018813, 74018815, 74018817.
Z-0010-2007 Smith & Nephew Inc 1
Genesis II Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71440480, 71440482, 71440484, 71440486
Z-0011-06 Stryker Howmedica Osteonics Corp. 1
Allocraft TLIF Bone Inserter.
Z-0011-2007 Smith & Nephew Inc 1
Genesis II Oversized Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71927102, 71927103, 71927104, 71927105
Z-0013-2011 Depuy Orthopaedics, Inc. 1
Summit Broach Handle, NON-STERILE, MFG: DEPUY ORTHOPAEDICS, INC., PO BOX 988 WARSAW, IN 46581, 1 800 366 8143 Catalog Number: 2570-00-000 The Summit Broach Handle (instrumentation) is used with the DePuy Summit Tapered Hip System. The Broach Handle is used to prepare the femur for hip system implantation. The broach handle is an impaction/extraction device that holds broaches for creating the cavity in the femur during hip arthroplasty.

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3030089866 ORTOLOG MEDIKAL SANAYI VE TICARET A.S. Yenimahalle Ankara, TR
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010806484. Last updated year: 2026. Please use registration number 3010806484 when referencing this establishment in official correspondence.
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