Signal Medical Corporation
Signal Medical Corporation holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2021, with 3 FDA device recalls on record.
Top product codes for Signal Medical Corporation
FDA recalls by Signal Medical Corporation
- Z-1834-2017 — Soft Face "No Bounce" Mallet Model/Catalog: BIO-1-1090
- Z-0111-2015 — Symmetric Total Knee Femoral Components Product Usage: Symmetric Total Knee Femoral Component is intended for use with Signal Medical Corp. Total Knee System for cemented use INA Total Knee Replacement. The femoral component is made of cobalt chromium alloy (ASTM F75).
- Z-0109-2015 — Microseal Augmented (20 degrees) Liner, acetabular liner component made from UHMW polyethylene (ASTM F648). Sizes 36x52x20; and 36x50x20. Device is intended for use with Whiteside Biomechanics, Inc./Signal Medical Corporation Micro-Seal Shell in an uncemented Total Hip Replacement.
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 Signal Medical Corporation
Data sourced from openFDA. This site is unofficial and independent of the FDA.