Data / Medical devices / France / Euclide Care

Euclide Care: FDA-registered device maker in Aixe Sur Vienne Haute-Vienne, France, 1 510(k) clearance

Name: Euclide Care FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Euclide Care is registered with the FDA (registration 3010370554) in Aixe Sur Vienne Haute-Vienne, France. It lists 16 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 18, 2017. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this one Watch Euclide Care

FDA registration number: 3010370554
Address: ZI Du Moulin Cheyroux, Aixe Sur Vienne Haute-Vienne, France, 87700
Owner or operator: Euclide Care (10043426)
Roles: Contract manufacturer, Exporter to the US
First device listed: February 14, 2013
Registered through: 2026
Brand names listed: Anterior blade, Array assembly, CC blade, CC lenghtening Shim, Cascadia AN Q Trial, Cascadia AN Q trial, Distal slider, End effector tube and more

Devices it lists

Device	Product code	Class	Role	Source
Appliance, Fixation, Spinal Interlaminal	KWP	2	Contract manufacturer	accessdata.fda.gov
Appliance, Fixation, Spinal Intervertebral Body	KWQ	2	Contract manufacturer	accessdata.fda.gov
Electrode, Needle	GXZ	2	Contract manufacturer	accessdata.fda.gov
Instrument, Manual, Surgical, General Use	MDM	1	Contract manufacturer, Exporter to the US	accessdata.fda.gov
Intervertebral Fusion Device With Bone Graft, Lumbar	MAX	2	Contract manufacturer	accessdata.fda.gov
Intervertebral Fusion Device With Integrated Fixation, Lumbar	OVD	2	Contract manufacturer	accessdata.fda.gov
Neurological Stereotaxic Instrument	HAW	2	Contract manufacturer	accessdata.fda.gov
Orthopedic Manual Surgical Instrument	LXH	1	Contract manufacturer, Exporter to the US	accessdata.fda.gov
Orthopedic Stereotaxic Instrument	OLO	2	Contract manufacturer, Exporter to the US	accessdata.fda.gov
Orthosis, Spinal Pedicle Fixation	MNI	2	Contract manufacturer	accessdata.fda.gov
Orthosis, Spondylolisthesis Spinal Fixation	MNH	2	Contract manufacturer	accessdata.fda.gov
Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis	OSH	2	Contract manufacturer	accessdata.fda.gov
Retractor	GAD	1	Contract manufacturer, Exporter to the US	accessdata.fda.gov
Syringe, Piston	FMF	2	Contract manufacturer	accessdata.fda.gov
Tap, Bone	HWX	1	Contract manufacturer	accessdata.fda.gov
Thoracolumbosacral Pedicle Screw System	NKB	2	Contract manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
October 18, 2017	K172034	Stryker Spine Navigation System with SpineMap 3D software application, OrthoLock, nGenius Spine Clamp, Navigated Drill Guide Set, Navigated Xia 3 Awl Tap, Navigated Xia 3 Serrato Tap	OLO	Substantially Equivalent	Stryker Corporation	accessdata.fda.gov

Compare with other makers

Updated October 18, 2017. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.