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BizLink Robotic Solutions France

Chartres Eure-et-Loir, FR

BizLink Robotic Solutions France appears in FDA device records in Chartres Eure-et-Loir, FR. FDA records list no 510(k) clearances, no PMA records and one registered establishment. As of , FDA records show 2 recalls for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
0
PMA records
0
Recall records
2
Registered establishments
1

FDA records under these names

1 name

FDA records resolved to BizLink Robotic Solutions France carry these names as well, as FDA wrote them. Each is the firm named on a registration, a 510(k), a PMA, a recall or an enforcement report that was joined to this company on a shared FDA identifier or on a matching name.

  • LEONI CIA CABLE SYSTEMSenforcement report, recall

510(k) clearance history

No 510(k) clearance records for this company in the ingested FDA data.

No 510(k) clearance records in the ingested FDA data.

Registered establishments

FDA registered establishments for BizLink Robotic Solutions France, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30128343723012834372BizLink Robotic Solutions France5 avenue Victor Hugo, Chartres Eure-et-Loir 28000 FR2026

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

Device recall records naming this company, most recent first
RecallProductReasonClassificationInitiatedStatus
Z-0399-2024ORION System with software OSS v6.0 and OSS v7.0- An electro-mechanical robotic arm for patient positioning in Radiation Therapy, Radiology, or Radiology image-guided treatment environment. Part Number: 1SOPT00009Users of the patient positioning system ORION System can be faced with a sudden short-term acceleration or with an unintended short-distance movement when the movements are again allowed after an unforeseen interruption signal of motion may result in a collision of the patient with another stationary component of the treatment room.Class IIOpen, Classified
Z-0398-2024ORION System with software OSS v6.0 and OSS v7.0- An electro-mechanical robotic arm for patient positioning in Radiation Therapy, Radiology, or Radiology image-guided treatment environment. Part Number: 1SOPT00003Users of the patient positioning system ORION System can be faced with a sudden short-term acceleration or with an unintended short-distance movement when the movements are again allowed after an unforeseen interruption signal of motion may result in a collision of the patient with another stationary component of the treatment room.Class IIOpen, Classified

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain