Allen Medical Systems, Inc.
Allen Medical Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 1997, with 3 FDA device recalls on record.
Top product codes for Allen Medical Systems, Inc.
FDA recalls by Allen Medical Systems, Inc.
- Z-1198-2017 — Arthrex Shoulder Suspension Tower; Catalog Number: AR-1650-01 Product Usage: The Arthrex Lateral Decubitus Shoulder Positioner is intended to allow for the controlled manipulation of the arm and shoulder joint during arthroscopic surgical procedures.
- Z-0928-2017 — Arthex S3 Arm Sleeve Connector; Catalog Number AR-1650-02; manufactured and distributed between March and November 2016.
- Z-0959-2013 — Allen Traction Boot, Modular, OT 1000 Traction Device Boot Assembly, Fracture Table Orthopedic Leg Holders, non-invasive medical devices designed to attach to orthopedic fracture tables to aid clinical staff in applying traction to the leg of a patient during surgical procedures.
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 Allen Medical Systems, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.