Home › SIGNUS Medizintechnik GmbH › MOBIS II 5°

MOBIS II 5°

SIGNUS Medizintechnik GmbH · Model Lumbar cage, angled · UDI-DI 04047844016145

MAX Prescription

510(k) clearances

9,183

Adverse events (30 deaths)

115

Recalls

422

Facilities

Description

The MOBIS II ST Spinal Implants have a hollow, slightly curved frame with areas of an open-pore titanium grid structure. Restoration of the intervertebral space can be achieved by the large selection of implants that, at the same time, offers a high degree of intraoperative flexibility. In addition to straight implants, the MOBIS II ST cage is alos avaible with a 5° lordoctic angle. Due to its design, the implant can be aligned with the anterior curvature of the intervertebral body and so is suited for unilateral, dorsal access (TLIF) in the L2 to S1 region of the spine.

Recalls

Date	Firm	Reason
2025-11-03	Orthofix U.S. LLC	Labeling contains claims that are not consistently present.
2025-11-03	Orthofix U.S. LLC	Labeling contains claims that are not consistently present.
2025-10-29	Medicrea International	Due to complaints, orthopedic rotation tool handle may untread from the shaft resulting in the inability to rotate implant.
2025-10-29	Medicrea International	Due to complaints, orthopedic rotation tool handle may untread from the shaft resulting in the inability to rotate implant.
2025-09-16	Medtronic Sofamor Danek USA Inc	Expandable interbody system cage may loose height or collapse (loss of lordosis), which could result in migration, subsidence and/or neurological injury. Therefore, surgical techni
2025-08-06	SEASPINE ORTHOPEDICS CORPORATION	Inserter, used as part of a system with an intervertebral body fusion device, may contribute to difficulty disengaging the implant or improper implant positioning, which may may le
2025-06-24	Orthofix U.S. LLC	A 37 mm implant width intervertebral body fusion device has a labeling discrepancy with incorrect width of 33 mm stated on the outer label side flap and inner label side flap infor
2025-02-20	Orthofix U.S. LLC	The product is mislabeled with the incorrect anterior height of 10mm, but the laser marking on the implant and corresponding trial both show the correct anterior height of 10.5mm.
2024-12-15	Alphatec Spine, Inc.	Complaints have been received regarding post-operative implant collapse.
2024-08-14	Innovasis, Inc	Due to interfacing issues between the implant trial and inserter of the lumbar intervertebral fusion device.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

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.