Orthofix Us L L C

FDA Filings

This page includes the latest FDA filings for Orthofix Us L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Filings

Device Company	Device	Date
GUDID 18257200140114 Orthofix US LLC	Firebird SI Fusion	2024-12-20
GUDID 18257200140107 Orthofix US LLC	Firebird SI Fusion	2024-12-20
GUDID 18257200158720 Orthofix US LLC	AccelStim 4300 Casting Kit Large	2023-06-20
GUDID 18257200158713 Orthofix US LLC	AccelStim 4300 Casting Kit Medium	2023-06-20
GUDID 18257200158706 Orthofix US LLC	AccelStim 4300 Casting Kit Small	2023-06-20
PMN K211712 Orthofix US LLC	3° Anterior Cervical Plating System, Reliant Anterior Cervical Plating System, Unity Lumbosacral Fixation System, Hallmark Anterior Plate System, NewBridge Laminoplasty Fixation System, CETRA Anterior Cervical Plate System	2022-02-11
PMN K213951 Orthofix US LLC	FORZA XP Expandable Spacer System	2022-01-05

Similar & Related FDA Registered Companies

• Orthofix US LLC3451 Plano Parkwaylewisville, TX 75056 PMA NumberP210035 Date Received10/13/2021 Decision Date05/03/2022 Product Code LOF  Advisory Committee Orthopedic Expedited Review Granted? No