BizLink Robotic Solutions France

FDA Device Registration & Listing · Chartres Eure-et-Loir, FR · Registration 3012834372

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
3012834372
FEI Number
3012834372
Entity Name
BizLink Robotic Solutions France
City/State/Country
Chartres Eure-et-Loir, FR
Establishment Address
5 avenue Victor Hugo, Chartres Eure-et-Loir 28000, FR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
BizLink Robotic Solutions France (Owner Number: 10055323)
Owner / Operator Contact Address
1 avenue Louis Pasteur, Zone industrielle de Gellainville, Gellainville, FR-28 28630, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Orion System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JAI Couch, Radiation Therapy, Powered Radiology Class 2 892.5770 2017-07-07

Official Correspondent

No official correspondent registered.

US Agent Details

Gregory LARSON Business: BizLink Robotic Solutions USA Email: gregory_larson@bizlinktech.com Phone: (248) 4845549

Related Public Records

Same Entity

BizLink Robotic Solutions France
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
K033316 Brainlab AG TABLE TILT DEVICE 2004-05-14

Similar Registrations

Registration Number Establishment Name Location
1932738 MEDTEC LLC Orange City, IA, US
2247992 Anholt Technologies Inc. Avondale, PA, US
3015232217 ELEKTA SOLUTIONS AB STOCKHOLM, SE
2436865 AKTINA MEDICAL CORP. Congers, NY, US
9710332 3C-Medical Intelligence GmbH Landsberg am Lech Bavaria, DE
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012834372. Last updated year: 2026. Please use registration number 3012834372 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.