32 results · 17ms · Sources: EU EUDAMED, US FDA

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T1040 AKA AURAWAVE

FDA 510(k)
FDA Class 2 ·Neurology

NATUS MEDICAL INCORPORATED DBA EXCEL-TECH LTD (XLTEK)

Manufacturer
🇨🇦 Canada·4 Importers

Dominion Biologicals Limited

Manufacturer
🇨🇦 Canada·TÜV Rheinland LGA Products GmbH

HANSAmed Limited DBA Citagenix

FDA registration
HANSAmed Limited DBA Citagenix·18 products·🇨🇦 Canada

Digital Dental Laboratories, DBA Orthodent

FDA registration
Digital Dental Laboratories, DBA Orthodent·9 products·🇨🇦 Canada

DECTRONIQUE (1984) INC. DBA DECTRO INTERNATIONAL

FDA registration
DECTRONIQUE (1984) INC. DBA DECTRO INTERNATIONAL·3 products·🇨🇦 Canada

EPM GLOBAL SERVICES INC., DBA VEXOS

FDA registration
EPM GLOBAL SERVICES INC., DBA VEXOS·2 products·🇨🇦 Canada

CANADIAN SCIENTIFIC PRODUCTS LTD. DBA CSP MEDICAL

FDA registration
CANADIAN SCIENTIFIC PRODUCTS LTD. DBA CSP MEDICAL·1 product·🇨🇦 Canada

DERMA SCIENCES CANADA, INC (dba DERMA SCIENCES, INC.)

FDA registration
DERMA SCIENCES CANADA, INC (dba DERMA SCIENCES, INC.)·21 products·🇨🇦 Canada

NATUS MEDICAL INCORPORATED DBA EXCEL-TECH LTD. (XLTEK)

FDA registration
NATUS MEDICAL INCORPORATED DBA EXCEL-TECH LTD. (XLTEK)·20 products·🇨🇦 Canada

AG MARKETING & DEVELOPMENT GROUP INC DBA AGMD GROUP

FDA registration
AG MARKETING & DEVELOPMENT GROUP INC DBA AGMD GROUP·26 products·🇨🇦 Canada

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

FDA registration
SPINOLOGICS, INC. also DBA Spino Modulation Inc and Numalogics Inc·1 product·🇨🇦 Canada

PrepIT Q2A Kit, Model PT-Q2A-96 containing component reagent AG (PT-QAG-96) 1.4mL and ST (PT-QST-96) 2.9mL - Product Usage: used for the removal of SDS and other inhibitors from samples collected using DNA Genotek oral sample collection kits.

FDA Enforcement
Class III ·Terminated·DNA Genotek Inc.·September 30, 2020

ORAcollect RNA: ORE-100

FDA Enforcement
Class II ·Ongoing·DNA Genotek Inc.·April 27, 2022

ORAcollect Dx, Catalog Number/SKU: OCD-100, OCD-100A. Material numbers: OCD-100, OCD-100.008, OCD-100.012, OCD-100.014+ACP078, OCD-100.014+ACP078, OCD-100.032 and OCD-100A, OCD-100A.022, OCD-100A.023, OCD-100A.024, OCD-100A.025

FDA Enforcement
Class II ·Ongoing·DNA Genotek Inc.·April 27, 2022

Navitrack¿ System - OS Knee Universal, Orthopedic Stereotaxic Instrument

FDA Enforcement
Class III ·Terminated·Orthosoft, Inc. dba Zimmer CAS·May 24, 2017

SmartTools Knee System Orthopedic Stereotaxic Instrument

FDA Enforcement
Class II ·Terminated·Orthosoft, Inc. dba Zimmer CAS·April 26, 2017

Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application intended to assist in the placement of total knee replacement components

FDA Enforcement
Class II ·Terminated·Orthosoft, Inc. dba Zimmer CAS·May 3, 2017

Navitrack System - OS Knee Universal, Stereotaxic instrument

FDA Enforcement
Class II ·Terminated·Orthosoft, Inc. dba Zimmer CAS·May 24, 2017

Sesamoid Plasty, Stereotaxic Instrument The Sesamoid Plasty workstation is used to run the tracking software as part of the software based navigation systems. The affected Sesamoid Plasty components are the central structural column and its base that hold up the computer and the tracking camera on the Sesamoid Plasty workstation. They are also designed to be disassembled such that the column can be folded onto itself for ease of transport after use. This is a retrospective recall report for a removal initiated on 17 June 2008

FDA Enforcement
Class II ·Terminated·Orthosoft, Inc. dba Zimmer CAS·June 14, 2017