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MEDITECH SPINE, LLC

Last updated May 23, 2026

Information

Page 108 of 108

Device	Model / Reference	Registries	Class	Status
Cure™ Acp	T-7-40042-34	FDA UDI	Class II	Active
Cure™ Acp	7-42141-18	FDA UDI	Class II	Active
Cure 2.0™ Acp	S1-10-00002-38	FDA UDI	Class II	Active
Cure™ Acp	T-7-40042-30	FDA UDI	Class II	Active
Cure Lp	9-00051-45	FDA UDI	Class II	Active
Cure Lp	9-41360-55	FDA UDI	Class II	Active
Cure™ Acp	7-00002-32	FDA UDI	Class II	Active
Cure™ Acp	700-400-01	FDA UDI	Class II	Active
Cure™ Acp	700-412-00	FDA UDI	Class II	Active
Cure Lp	S1-9-00011-34	FDA UDI	Class II	Active
Talos®-C Cervical Intervertebral Body Fusion System, Talos®-C (HA) Cervical Intervertebral Body Fusion System	K201506	FDA 510(k)	Class II	Active
Talos-C(HA) Cervical Intervertebral Body Fusion Devices	K142345	FDA 510(k)	Class II	Active
Cure™ Lumbar Plate System	K180090	FDA 510(k)	Class II	Active
Talos® Lumbar (HA) PEEK IBF Devices	K170395	FDA 510(k)	Class II	Active
Talos Intervertebral Body Fusion Devices, Talos -C Cervical Intervertebral Body Fusion Devices, Talos -C(HA) Cervical Intervertebral Body Fusion Devices	K150788	FDA 510(k)	Class II	Active
Cure™ Lumbar Plate System	K201136	FDA 510(k)	Class II	Active
Cure™ Lumbar Plate System	K171538	FDA 510(k)	Class II	Active
Cure 2.0 Anterior Cervical Plate (ACP) System	K210286	FDA 510(k)	Class II	Active
Cure™ Anterior Cervical Plate (ACP) System	K160604	FDA 510(k)	Class II	Active
Cure™ OPEL-C Plate System	K181543	FDA 510(k)	Class II	Active

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