FDA.report

SPINEVISION

FDA Registration(s)

RegistrationFEINameStatusInitial importerExpiration yearAddress
30254570953025457095SPINEVISION INC.1Y2026-01-012547 Farrington St Dallas TX US 75207
10671453010321861SPINEVISION, INC.1Y2020-04-25185 Alewife Brook Pkwy Ste 402 Cambridge MA US 02138

GUDID Contact Samples

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDIDProductPhoneEmail
03663136009308Hexanium® ACIF - Lordotic Ti Cervical Cage Trial Without Stop+33153332525corp.quality@spinevision.com
03663136009315Hexanium® ACIF - Lordotic Ti Cervical Cage Trial Without Stop+33153332525corp.quality@spinevision.com
03663136009322Hexanium® ACIF - Lordotic Ti Cervical Cage Trial Without Stop+33153332525corp.quality@spinevision.com

PMN

GUDID

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