Ulrich Medical USA, Inc.
Ulrich Medical USA, Inc. holds FDA 510(k) medical device clearances, first cleared 2024, most recent 2026, with 3 FDA device recalls on record.
Top product codes for Ulrich Medical USA, Inc.
FDA recalls by Ulrich Medical USA, Inc.
- Z-1350-2020 — Ulrich medical neon3 OCT spinal stabilization, REF CS 3917-12, Locking screw for crosslink, screw-to-screw
- Z-1126-2019 — ULRICH Torque Limiting Handle for use with a Set Screw Driver to perform the final tightening of set screws in a spinal implant construct.
- Z-1878-2017 — uNion Cervical Plate System Product Usage: The uNion Cervical Plate System is intended for anterior fixation of the cervical spine (C2 to Ti). The system is to be used to provide stabilization of the anterior cervical spine as an adjunct to fusion for the treatment of degenerative disc disease (defined as neck pain of discogenic origin with the degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fractures or dislocations), tumors, spinal stenosis, deformity (i.e., kyphosis, lordosis or scoliosis), pseudarthrosis or failed previous fusion.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Ulrich Medical USA, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.