FDA Device Intelligence
HomeSeaspine Orthopedics Corporation › Coral

Coral

Seaspine Orthopedics Corporation · Model 18-30-0080 · UDI-DI 10889981028091

NKBKWQMNIKWPMNH Prescription
1
510(k) clearances
24,738
Adverse events (86 deaths)
181
Recalls
409
Facilities

Description

Prebent Hex Rod 5.5 x 80mm. The Coral Spinal System consists of a variety of types and sizes of rods, hooks, screws, and connectors. The Coral Spinal System implant components can be rigidly locked into a variety of configurations that can be fit for the individual case. The Coral Spinal System components are manufactured from medical implant grade titanium alloy Ti-6Al-4V (ELI) per ASTM F-136, ASTM-F-67, and cobalt chrome alloy per ASTM F-1537.

Recalls

DateFirmReason
2026-05-28SEASPINE ORTHOPEDICS CORPORATIONDue to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion.
2026-05-22Innovasis, IncPedicle 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
2025-09-19Orthofix U.S. LLCPolyaxial screws do not meet performance standards.
2025-06-30SPINEART SACannulated fenestrated polyaxial screws may be incorrectly labeled
2025-06-30SPINEART SACannulated fenestrated polyaxial screws may be incorrectly labeled
2024-10-29SEASPINE ORTHOPEDICS CORPORATIONDue to manufacturing defects observed on Locking Caps that affect the ability for components to mate.
2024-10-29SEASPINE ORTHOPEDICS CORPORATIONDue to manufacturing defects observed on Locking Caps that affect the ability for components to mate.
2024-08-21XTANT Medical Holdings, IncSpinal 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
2024-03-15SPINEART SADue 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
2024-02-28SEASPINE ORTHOPEDICS CORPORATIONScrew heads, of pedicle screw systems, have partial thread within the screw head that pose a risk of intraoperative cross-threading within the locking cap/screw head interface.

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 keyRead 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.