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FOCUS

NVision Biomedical Technologies, Inc. · Model PDC-750-060 · UDI-DI 00814008026876

NKB Prescription

510(k) clearances

24,738

Adverse events (86 deaths)

182

Recalls

409

Facilities

Description

PS, MIS-Tower, Cannulated Cortical Cancellous 7.5X60mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion.

Recalls

Date	Firm	Reason
2026-08-19	SEASPINE ORTHOPEDICS CORPORATION	The proximal thread depth of the spinal device is out of design specification.
2026-05-28	SEASPINE ORTHOPEDICS CORPORATION	Due to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion.
2026-05-22	Innovasis, Inc	Pedicle screw system intended to provide immobilization/stabilization of spinal segments as adjunct to thoracic/lumbar/sacral spine fusion may have anti-torque instrument with unde
2025-09-19	Orthofix U.S. LLC	Polyaxial screws do not meet performance standards.
2025-06-30	SPINEART SA	Cannulated fenestrated polyaxial screws may be incorrectly labeled
2025-06-30	SPINEART SA	Cannulated fenestrated polyaxial screws may be incorrectly labeled
2024-10-29	SEASPINE ORTHOPEDICS CORPORATION	Due to manufacturing defects observed on Locking Caps that affect the ability for components to mate.
2024-10-29	SEASPINE ORTHOPEDICS CORPORATION	Due to manufacturing defects observed on Locking Caps that affect the ability for components to mate.
2024-08-21	XTANT Medical Holdings, Inc	Spinal fixation system implant screws marked "DNI" are not intended to be implanted and may not have been manufactured in accordance with released manufacturing specifications, and
2024-03-15	SPINEART SA	Due to receiving information regarding difficulties with the insertion of a setscrew inside a screw head. Issues involved, either: 1. The setscrew is not tightened to torque 2. The

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.